665
659
4
http://purl.obolibrary.org/obo/MONDO_0021500
benign neoplasm of spleen
'benign neoplasm of spleen' SubClassOf 'digestive system neoplasm'
'benign neoplasm of spleen' SubClassOf 'splenic disease'
'benign neoplasm of spleen' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036696
http://purl.obolibrary.org/obo/MONDO_0021547
amelogenesis imperfecta type 3B
http://purl.obolibrary.org/obo/DOID_0080243 EquivalentTo 'amelogenesis imperfecta type 3B'
http://purl.obolibrary.org/obo/MONDO_0021439
benign neoplasm of pituitary gland
'benign neoplasm of pituitary gland' SubClassOf 'pituitary gland disease'
'benign neoplasm of pituitary gland' SubClassOf 'connective tissue benign neoplasm'
'benign neoplasm of pituitary gland' SubClassOf 'pituitary tumor'
http://purl.obolibrary.org/obo/MONDO_0011929
chromosome 1p36 deletion syndrome
'chromosome 1p36 deletion syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'chromosome 1p36 deletion syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0011960
schizophrenia 11
'schizophrenia 11' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070087 EquivalentTo 'schizophrenia 11'
'schizophrenia 11' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0011961
hereditary sensory and autonomic neuropathy type 1B
http://purl.obolibrary.org/obo/DOID_0070148 EquivalentTo 'hereditary sensory and autonomic neuropathy type 1B'
http://purl.obolibrary.org/obo/MONDO_0021312
malignant tumor of adrenal cortex
'malignant tumor of adrenal cortex' SubClassOf 'adrenal cortex disease'
'malignant tumor of adrenal cortex' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036591
http://purl.obolibrary.org/obo/MONDO_0011821
Meckel syndrome, type 3
'Meckel syndrome, type 3' SubClassOf 'Meckel syndrome'
'Meckel syndrome, type 3' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070117 EquivalentTo 'Meckel syndrome, type 3'
http://purl.obolibrary.org/obo/MONDO_0011849
psoriatic arthritis
'psoriatic arthritis' EquivalentTo 'arthritis' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445) and ('disease has major feature' some 'psoriasis')
'psoriatic arthritis' EquivalentTo 'arthritis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960) and ('disease has major feature' some 'psoriasis')
http://purl.obolibrary.org/obo/MONDO_0021202
allergic otitis media
'allergic otitis media' SubClassOf 'disease disrupting biological or physiological process'
'allergic otitis media' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0016068
'allergic otitis media' SubClassOf 'allergic disease'
http://purl.obolibrary.org/obo/MONDO_0011871
Niemann-Pick disease type B
'Niemann-Pick disease type B' SubClassOf 'Niemann-Pick disease'
'Niemann-Pick disease type B' SubClassOf 'Niemann-Pick disease'
http://purl.obolibrary.org/obo/DOID_0070112 EquivalentTo 'Niemann-Pick disease type B'
http://purl.obolibrary.org/obo/MONDO_0011873
Niemann-Pick disease, type C2
http://purl.obolibrary.org/obo/DOID_0070114 EquivalentTo 'Niemann-Pick disease, type C2'
http://purl.obolibrary.org/obo/MONDO_0021251
endometrium neoplasm
'endometrium neoplasm' SubClassOf 'tumor of uterus'
'endometrium neoplasm' SubClassOf 'tumor of uterus'
'endometrium neoplasm' EquivalentTo http://purl.obolibrary.org/obo/SCTID_123844007
http://purl.obolibrary.org/obo/MONDO_0021282
malignant teratoma of testis
'malignant teratoma of testis' SubClassOf 'testicular cancer'
'malignant teratoma of testis' SubClassOf 'testicular germ cell tumor'
'malignant teratoma of testis' SubClassOf 'malignant testicular germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0011715
Seckel syndrome 2
'Seckel syndrome 2' SubClassOf 'Seckel syndrome'
'Seckel syndrome 2' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070013 EquivalentTo 'Seckel syndrome 2'
http://purl.obolibrary.org/obo/MONDO_0011724
encephalopathy due to GLUT1 deficiency
'encephalopathy due to GLUT1 deficiency' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0011749
oculocutaneous albinism type 1B
http://purl.obolibrary.org/obo/DOID_0070095 EquivalentTo 'oculocutaneous albinism type 1B'
http://purl.obolibrary.org/obo/MONDO_0011740
Carney-Stratakis syndrome
'Carney-Stratakis syndrome' SubClassOf 'rare genetic endocrine disease'
'Carney-Stratakis syndrome' SubClassOf 'rare genetic inherited tumor'
http://purl.obolibrary.org/obo/MONDO_0011794
Dravet syndrome
'Dravet syndrome' SubClassOf 'infantile epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0021138
bone marrow cancer
'bone marrow cancer' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/MONDO_0011676
PHACE syndrome
'PHACE syndrome' SubClassOf 'rare genetic epilepsy'
'PHACE syndrome' SubClassOf 'brain neoplasm'
http://purl.obolibrary.org/obo/MONDO_0011683
oculocutaneous albinism type 4
'oculocutaneous albinism type 4' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/DOID_0070098 EquivalentTo 'oculocutaneous albinism type 4'
'oculocutaneous albinism type 4' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/DOID_0050923
http://purl.obolibrary.org/obo/DOID_0050923 EquivalentTo 'spindle epithelial tumor with thymus-like differentiation tumor'
http://purl.obolibrary.org/obo/DOID_0050923 EquivalentTo 'thyroid gland spindle cell tumor with thymus-like differentiation'
http://purl.obolibrary.org/obo/MONDO_0021054
bone sarcoma
'bone sarcoma' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0021081
anti-NMDA receptor encephalitis
'anti-NMDA receptor encephalitis' SubClassOf 'rare epilepsy'
'anti-NMDA receptor encephalitis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100029
http://purl.obolibrary.org/obo/DOID_6917
http://purl.obolibrary.org/obo/DOID_6917 EquivalentTo 'predominantly cortical thymoma'
http://purl.obolibrary.org/obo/DOID_6917 EquivalentTo 'thymoma type B1'
http://purl.obolibrary.org/obo/MONDO_0011552
SCZD10
'SCZD10' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070086 EquivalentTo 'SCZD10'
'SCZD10' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0011576
familial hyperaldosteronism type II
'familial hyperaldosteronism type II' SubClassOf 'adrenal gland neoplasm'
'familial hyperaldosteronism type II' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036591
http://purl.obolibrary.org/obo/MONDO_0011583
cerebral amyloid angiopathy, App-related
'cerebral amyloid angiopathy, App-related' SubClassOf 'cerebral amyloid angiopathy'
http://purl.obolibrary.org/obo/DOID_0070028 EquivalentTo 'cerebral amyloid angiopathy, App-related'
'cerebral amyloid angiopathy, App-related' SubClassOf 'cerebral amyloid angiopathy'
http://purl.obolibrary.org/obo/MONDO_0011424
Carney triad
'Carney triad' SubClassOf 'hereditary neoplastic syndrome'
'Carney triad' SubClassOf 'has modifier' some 'acquired'
'Carney triad' SubClassOf 'neoplastic syndrome'
http://purl.obolibrary.org/obo/MONDO_0011479
orthostatic intolerance
'orthostatic intolerance' SubClassOf 'heart conduction disease'
'orthostatic intolerance' SubClassOf 'rare genetic cardiac disease'
http://purl.obolibrary.org/obo/DOID_0111154 EquivalentTo 'orthostatic intolerance'
http://purl.obolibrary.org/obo/MONDO_0011498
schizophrenia 9
'schizophrenia 9' SubClassOf 'schizophrenia (disease)'
'schizophrenia 9' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070085 EquivalentTo 'schizophrenia 9'
http://purl.obolibrary.org/obo/MONDO_0006745
endometrioid stromal sarcoma
'endometrioid stromal sarcoma' SubClassOf 'endometrial cancer'
http://purl.obolibrary.org/obo/MONDO_0006785
Henoch-Schoenlein purpura
'Henoch-Schoenlein purpura' SubClassOf 'vasculitis'
'Henoch-Schoenlein purpura' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/MONDO_0006799
hypothalamic neoplasm
'hypothalamic neoplasm' EquivalentTo 'thalamic cancer' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_2000364)
'hypothalamic neoplasm' SubClassOf 'thalamic cancer'
'hypothalamic neoplasm' SubClassOf 'bone cancer'
'hypothalamic neoplasm' SubClassOf 'connective tissue neoplasm'
'hypothalamic neoplasm' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0001898
'hypothalamic neoplasm' SubClassOf 'brain neoplasm'
'hypothalamic neoplasm' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001898)
http://purl.obolibrary.org/obo/MONDO_0006794
hypersensitivity vasculitis
'hypersensitivity vasculitis' SubClassOf 'hypersensitivity reaction type III disease'
'hypersensitivity vasculitis' SubClassOf 'rare immune disease'
'hypersensitivity vasculitis' SubClassOf 'hypersensitivity reaction disease'
'hypersensitivity vasculitis' SubClassOf 'vasculitis'
http://purl.obolibrary.org/obo/MONDO_0016169
chronic acquired demyelinating polyneuropathy
'chronic acquired demyelinating polyneuropathy' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic acquired demyelinating polyneuropathy' EquivalentTo 'acquired peripheral neuropathy' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
http://purl.obolibrary.org/obo/MONDO_0016167
optic pathway glioma
'optic pathway glioma' SubClassOf 'brain neoplasm'
'optic pathway glioma' SubClassOf 'rare tumor of endocrine glands'
'optic pathway glioma' SubClassOf 'pituitary tumor'
http://purl.obolibrary.org/obo/MONDO_0006685
brain hypoxia-ischemia
'brain hypoxia-ischemia' SubClassOf 'brain disease'
'brain hypoxia-ischemia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/MONDO_0016019
Rasmussen subacute encephalitis
'Rasmussen subacute encephalitis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100028
http://purl.obolibrary.org/obo/MONDO_0016022
early myoclonic encephalopathy
'early myoclonic encephalopathy' SubClassOf 'neonatal epilepsy syndrome'
'early myoclonic encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100022
http://purl.obolibrary.org/obo/MONDO_0016025
myoclonic-astastic epilepsy
'myoclonic-astastic epilepsy' SubClassOf 'childhood-onset epilepsy syndrome'
'myoclonic-astastic epilepsy' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0016021
early infantile epileptic encephalopathy
'early infantile epileptic encephalopathy' SubClassOf 'neonatal epilepsy syndrome'
'early infantile epileptic encephalopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100022
http://purl.obolibrary.org/obo/MONDO_0006500
hemangioma
'hemangioma' SubClassOf 'epithelial neoplasm'
'hemangioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0006536
congenital generalized lipodystrophy (disease)
'congenital generalized lipodystrophy (disease)' SubClassOf 'lipodystrophy (disease)'
'congenital generalized lipodystrophy (disease)' SubClassOf 'genetic lipodystrophy'
'congenital generalized lipodystrophy (disease)' SubClassOf http://purl.obolibrary.org/obo/MONDO_0027766
'congenital generalized lipodystrophy (disease)' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0027766 and ('has modifier' some 'genetic and inherited')
http://purl.obolibrary.org/obo/MONDO_0006558
pemphigoid gestationis
http://purl.obolibrary.org/obo/DOID_0040098 EquivalentTo 'pemphigoid gestationis'
http://purl.obolibrary.org/obo/MONDO_0006573
lipodystrophy (disease)
'lipodystrophy (disease)' EquivalentTo 'disease' and ('disease has major feature' some http://purl.obolibrary.org/obo/HP_0009125)
'lipodystrophy (disease)' SubClassOf 'disease has major feature' some http://purl.obolibrary.org/obo/HP_0009125
http://purl.obolibrary.org/obo/MONDO_0006416
small intestinal Burkitt lymphoma
'small intestinal Burkitt lymphoma' SubClassOf 'rare bone disease'
'small intestinal Burkitt lymphoma' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0006459
thymoma type B1
'thymoma type B1' SubClassOf 'thymoma type B'
http://linkedlifedata.com/resource/umls/id/C1266094 EquivalentTo 'thymoma type B1'
http://purl.obolibrary.org/obo/DOID_6917 EquivalentTo 'thymoma type B1'
'thymoma type B1' SubClassOf 'thymoma type B'
http://purl.obolibrary.org/obo/MONDO_0006466
thyroid gland spindle cell tumor with thymus-like differentiation
'thyroid gland spindle cell tumor with thymus-like differentiation' SubClassOf 'hemangiopericytoma'
http://purl.obolibrary.org/obo/DOID_0050923 EquivalentTo 'thyroid gland spindle cell tumor with thymus-like differentiation'
'thyroid gland spindle cell tumor with thymus-like differentiation' SubClassOf 'thyroid gland carcinoma'
http://purl.obolibrary.org/obo/MONDO_0006487
vaginal adenoid cystic carcinoma
'vaginal adenoid cystic carcinoma' SubClassOf 'vaginal glandular neoplasm'
http://purl.obolibrary.org/obo/MONDO_0006493
Warthin tumor
'Warthin tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0021950
autoimmune oophoritis
'autoimmune oophoritis' EquivalentTo 'oophoritis' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune oophoritis' SubClassOf 'disease disrupting biological or physiological process'
'autoimmune oophoritis' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445
'autoimmune oophoritis' EquivalentTo 'oophoritis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune oophoritis' SubClassOf 'autoimmune disease of endocrine system'
http://purl.obolibrary.org/obo/MONDO_0006373
pituitary gland adenoma
'pituitary gland adenoma' SubClassOf 'benign neoplasm of pituitary gland'
'pituitary gland adenoma' SubClassOf 'connective tissue benign neoplasm'
http://purl.obolibrary.org/obo/COHD_372652
http://purl.obolibrary.org/obo/COHD_372652 EquivalentTo 'chronic tympanitis'
http://purl.obolibrary.org/obo/COHD_372652 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0001227ub
http://purl.obolibrary.org/obo/MONDO_0006281
lung signet ring cell carcinoma
'lung signet ring cell carcinoma' SubClassOf 'lung adenocarcinoma'
'lung signet ring cell carcinoma' SubClassOf 'lung adenocarcinoma'
http://purl.obolibrary.org/obo/DOID_0080305 EquivalentTo 'lung signet ring cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0006290
malignant germ cell tumor
'malignant germ cell tumor' SubClassOf 'mixed germ cell cancer'
'malignant germ cell tumor' EquivalentTo 'cancer' and ('disease has location' some http://purl.obolibrary.org/obo/CL_0000586)
'malignant germ cell tumor' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/CL_0000586
'malignant germ cell tumor' SubClassOf 'cancer'
'malignant germ cell tumor' SubClassOf 'germ cell tumor'
'malignant germ cell tumor' EquivalentTo 'germ cell tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
http://purl.obolibrary.org/obo/MONDO_0006291
malignant jugulotympanic paraganglioma
'malignant jugulotympanic paraganglioma' SubClassOf 'vascular bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0006298
mediastinal malignant germ cell tumor
'mediastinal malignant germ cell tumor' SubClassOf 'mixed germ cell cancer'
'mediastinal malignant germ cell tumor' SubClassOf 'malignant germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0006103
benign adrenal gland pheochromocytoma
'benign adrenal gland pheochromocytoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0006123
cardiac rhabdomyoma (disease)
'cardiac rhabdomyoma (disease)' SubClassOf 'rhabdomyosarcoma (disease)'
'cardiac rhabdomyoma (disease)' SubClassOf 'heart sarcoma'
'cardiac rhabdomyoma (disease)' EquivalentTo 'rhabdomyosarcoma (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000948)
'cardiac rhabdomyoma (disease)' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0036688 and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000948)
'cardiac rhabdomyoma (disease)' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036688
'cardiac rhabdomyoma (disease)' SubClassOf 'benign neoplasm of heart'
http://purl.obolibrary.org/obo/MONDO_0006144
cervical wilms tumor
'cervical wilms tumor' SubClassOf 'cervical cancer'
http://purl.obolibrary.org/obo/DOID_5190 EquivalentTo 'cervical wilms tumor'
'cervical wilms tumor' SubClassOf 'cervical carcinosarcoma'
http://linkedlifedata.com/resource/umls/id/C1516437 EquivalentTo 'cervical wilms tumor'
'cervical wilms tumor' EquivalentTo 'Wilms tumor' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000002)
http://purl.obolibrary.org/obo/MONDO_0006150
colon Burkitt lymphoma
'colon Burkitt lymphoma' SubClassOf 'rare bone disease'
'colon Burkitt lymphoma' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/DOID_0080098
http://purl.obolibrary.org/obo/DOID_0080098 EquivalentTo 'fatal infantile hypertonic myofibrillar myopathy'
http://purl.obolibrary.org/obo/DOID_0080098 EquivalentTo 'myofibrillar myopathy 7'
http://purl.obolibrary.org/obo/MONDO_0006021
Prinzmetal's angina
'Prinzmetal's angina' SubClassOf 'cardiovascular disease'
'Prinzmetal's angina' SubClassOf 'coronary vasospasm'
http://purl.obolibrary.org/obo/DOID_0111151 EquivalentTo 'Prinzmetal's angina'
http://purl.obolibrary.org/obo/MONDO_0021666
ear infection
'ear infection' SubClassOf 'post-infectious disorder'
'ear infection' SubClassOf 'disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0001690
'ear infection' EquivalentTo 'disease' and ('disease arises from feature' some 'infectious disease') and ('disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0001690)
'ear infection' SubClassOf 'rare otorhinolaryngologic disease'
'ear infection' SubClassOf 'infectious disease of the nervous system'
'ear infection' EquivalentTo 'infectious disease' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001690)
http://purl.obolibrary.org/obo/MONDO_0006031
chronic rhinosinusitis
'chronic rhinosinusitis' EquivalentTo 'sinusitis' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
'chronic rhinosinusitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
http://purl.obolibrary.org/obo/MONDO_0006079
ameloblastic carcinoma
'ameloblastic carcinoma' SubClassOf 'bone cancer'
'ameloblastic carcinoma' SubClassOf 'bone carcinoma'
http://purl.obolibrary.org/obo/MONDO_0002363
papilloma
'papilloma' SubClassOf 'benign neoplasm'
'papilloma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0002370
ovarian Brenner tumor
'ovarian Brenner tumor' SubClassOf 'ovarian neoplasm'
'ovarian Brenner tumor' SubClassOf 'ovarian epithelial tumor'
http://purl.obolibrary.org/obo/MONDO_0002398
mucinous adenofibroma
'mucinous adenofibroma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0002395
renal adenoma
'renal adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0002415
bone carcinoma
'bone carcinoma' SubClassOf 'bone disease'
http://purl.obolibrary.org/obo/MONDO_0002416
ethmoid sinus squamous cell carcinoma
'ethmoid sinus squamous cell carcinoma' SubClassOf 'rare nervous system tumor'
'ethmoid sinus squamous cell carcinoma' SubClassOf 'rare bone disease'
'ethmoid sinus squamous cell carcinoma' SubClassOf 'rare respiratory disease'
'ethmoid sinus squamous cell carcinoma' SubClassOf 'bone squamous cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0002422
adamantinoma
'adamantinoma' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0002459
hypersensitivity reaction type IV disease
'hypersensitivity reaction type IV disease' SubClassOf 'hypersensitivity reaction disease'
http://linkedlifedata.com/resource/umls/id/C0021070 EquivalentTo 'hypersensitivity reaction type IV disease'
'hypersensitivity reaction type IV disease' EquivalentTo 'immune system disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0001806)
'hypersensitivity reaction type IV disease' EquivalentTo 'disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0001806)
'hypersensitivity reaction type IV disease' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3115
http://linkedlifedata.com/resource/umls/id/C0020522 EquivalentTo 'hypersensitivity reaction type IV disease'
'hypersensitivity reaction type IV disease' SubClassOf 'hypersensitivity reaction type II disease'
http://purl.obolibrary.org/obo/MONDO_0002450
prostatic adenoma
'prostatic adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0002451
benign prostate phyllodes tumor
'benign prostate phyllodes tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037002
http://linkedlifedata.com/resource/umls/id/C0395849
http://linkedlifedata.com/resource/umls/id/C0395849 EquivalentTo 'chronic tympanitis'
http://linkedlifedata.com/resource/umls/id/C0395849 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0001227ub
http://purl.obolibrary.org/obo/MONDO_0002301
frontal sinus squamous cell carcinoma
'frontal sinus squamous cell carcinoma' SubClassOf 'rare respiratory disease'
'frontal sinus squamous cell carcinoma' SubClassOf 'rare nervous system tumor'
'frontal sinus squamous cell carcinoma' SubClassOf 'rare bone disease'
'frontal sinus squamous cell carcinoma' SubClassOf 'bone squamous cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0016955
partial duplication of the long arm of chromosome 4
http://purl.obolibrary.org/obo/DOID_0111159 EquivalentTo 'partial duplication of the long arm of chromosome 4'
'partial duplication of the long arm of chromosome 4' SubClassOf 'syndrome caused by partial chromosomal duplication'
http://purl.obolibrary.org/obo/MONDO_0002335
chronic inflammatory demyelinating polyneuritis
'chronic inflammatory demyelinating polyneuritis' EquivalentTo 'demyelinating polyneuropathy' and 'inflammatory disease' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
'chronic inflammatory demyelinating polyneuritis' SubClassOf 'chronic polyneuropathy'
http://purl.obolibrary.org/obo/MONDO_0002336
inflammatory and toxic neuropathy
'inflammatory and toxic neuropathy' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0016742
mixed germ cell tumor of central nervous system
'mixed germ cell tumor of central nervous system' SubClassOf 'mixed germ cell tumor'
'mixed germ cell tumor of central nervous system' SubClassOf 'mixed extragonadal germ cell cancer'
http://purl.obolibrary.org/obo/MONDO_0002109
pituitary cancer
'pituitary cancer' EquivalentTo http://purl.obolibrary.org/obo/SCTID_127024001
'pituitary cancer' SubClassOf 'diencephalic cancer'
'pituitary cancer' EquivalentTo 'supratentorial cancer' and 'cancer' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000007)
'pituitary cancer' SubClassOf 'pituitary tumor'
'pituitary cancer' EquivalentTo 'cancer' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000007)
'pituitary cancer' EquivalentTo http://purl.obolibrary.org/obo/SCTID_363482009
'pituitary cancer' SubClassOf 'pituitary tumor'
'pituitary cancer' SubClassOf 'thalamic cancer'
http://purl.obolibrary.org/obo/MONDO_0002110
adrenal rest tumor
'adrenal rest tumor' SubClassOf 'benign reproductive system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0002129
bone cancer
'bone cancer' SubClassOf 'skeletal system disease'
'bone cancer' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0004765
'bone cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4016
'bone cancer' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0002131
jaw cancer
'jaw cancer' SubClassOf 'rare gastroenterologic disease'
'jaw cancer' SubClassOf 'rare digestive tumor'
http://purl.obolibrary.org/obo/MONDO_0002132
skull cancer
'skull cancer' SubClassOf 'rare head and neck tumor'
http://purl.obolibrary.org/obo/MONDO_0002197
minor vestibular glands adenoma
'minor vestibular glands adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/OMIM_610253
'Kleefstra syndrome' EquivalentTo http://purl.obolibrary.org/obo/OMIM_610253
http://purl.obolibrary.org/obo/MONDO_0027407 EquivalentTo http://purl.obolibrary.org/obo/OMIM_610253
http://purl.obolibrary.org/obo/MONDO_0002003
papilledema
'papilledema' SubClassOf 'optic nerve disease'
'papilledema' SubClassOf 'optic nerve disease'
http://purl.obolibrary.org/obo/MONDO_0002013
lymphangioma
'lymphangioma' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0001473
'lymphangioma' SubClassOf 'epithelial neoplasm'
'lymphangioma' SubClassOf 'vascular disease'
'lymphangioma' SubClassOf 'vascular neoplasm'
'lymphangioma' SubClassOf 'lymphatic system disease'
'lymphangioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
'lymphangioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036870
http://purl.obolibrary.org/obo/MONDO_0002029
chronic gonorrhea of cervix
'chronic gonorrhea of cervix' EquivalentTo 'gonococcal cervicitis' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
http://purl.obolibrary.org/obo/MONDO_0002058
breast adenoma
'breast adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0002065
benign breast adenomyoepithelioma
'benign breast adenomyoepithelioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0002082
endocrine gland neoplasm
'endocrine gland neoplasm' EquivalentTo http://purl.obolibrary.org/obo/SCTID_387922007
http://purl.obolibrary.org/obo/MONDO_0016733
ganglioglioma
'ganglioglioma' SubClassOf 'rare epilepsy'
'ganglioglioma' SubClassOf 'brain neoplasm'
'ganglioglioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/MONDO_0016532
Lennox-Gastaut syndrome
'Lennox-Gastaut syndrome' SubClassOf 'childhood-onset epilepsy syndrome'
'Lennox-Gastaut syndrome' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0016558
familial congenital mirror movements
http://purl.obolibrary.org/obo/DOID_0111153 EquivalentTo 'familial congenital mirror movements'
http://purl.obolibrary.org/obo/MONDO_0016407
oligomeganephronia
http://purl.obolibrary.org/obo/DOID_0111142 EquivalentTo 'oligomeganephronia'
http://purl.obolibrary.org/obo/MONDO_0016402
mitochondrial disease with epilepsy
'mitochondrial disease with epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/MONDO_0016474
drug-induced lupus erythematosus
'drug-induced lupus erythematosus' SubClassOf 'lupus erythematosus'
http://purl.obolibrary.org/obo/DOID_0040093 EquivalentTo 'drug-induced lupus erythematosus'
'drug-induced lupus erythematosus' SubClassOf 'lupus erythematosus'
http://purl.obolibrary.org/obo/MONDO_0016483
intracranial berry aneurysm
'intracranial berry aneurysm' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0006962
sebaceous adenocarcinoma
'sebaceous adenocarcinoma' SubClassOf 'sebaceous gland neoplasm'
'sebaceous adenocarcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037735
http://purl.obolibrary.org/obo/MONDO_0006823
Klinefelter syndrome
'Klinefelter syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0006890
parathyroid gland adenoma
'parathyroid gland adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0016218
Guillain-Barre syndrome
'Guillain-Barre syndrome' SubClassOf 'autoimmune disease of peripheral nervous system'
'Guillain-Barre syndrome' SubClassOf 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/MONDO_0016244
atypical hemolytic-uremic syndrome
'atypical hemolytic-uremic syndrome' SubClassOf 'syndromic disease'
http://purl.obolibrary.org/obo/GARD_0006240 EquivalentTo 'atypical hemolytic-uremic syndrome'
'atypical hemolytic-uremic syndrome' SubClassOf 'complement deficiency'
http://purl.obolibrary.org/obo/GARD_0008702 EquivalentTo 'atypical hemolytic-uremic syndrome'
'atypical hemolytic-uremic syndrome' SubClassOf 'rare genetic primary immunodeficiency'
http://purl.obolibrary.org/obo/DOID_0080301 EquivalentTo 'atypical hemolytic-uremic syndrome'
http://purl.obolibrary.org/obo/MONDO_0016253
rare cancer of corpus uteri
'rare cancer of corpus uteri' EquivalentTo 'cancer' and ('has modifier' some 'rare') and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0009853)
'rare cancer of corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016270
low-grade neuroendocrine tumor of the corpus uteri
'low-grade neuroendocrine tumor of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016268
papillary carcinoma of the corpus uteri
'papillary carcinoma of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016269
high-grade neuroendocrine carcinoma of the corpus uteri
'high-grade neuroendocrine carcinoma of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016264
autoimmune hepatitis
'autoimmune hepatitis' EquivalentTo 'hepatitis' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune hepatitis' EquivalentTo 'hepatitis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0016266
squamous cell carcinoma of the corpus uteri
'squamous cell carcinoma of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016267
undifferentiated carcinoma of the corpus uteri
'undifferentiated carcinoma of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016271
adenoid cystic carcinoma of the corpus uteri
'adenoid cystic carcinoma of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016272
transitional cell carcinoma of the corpus uteri
'transitional cell carcinoma of the corpus uteri' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0016273
malignant germ cell tumor of corpus uteri
'malignant germ cell tumor of corpus uteri' SubClassOf 'uterine corpus cancer'
http://www.ebi.ac.uk/efo/EFO_0005809
'hypersensitivity reaction type II disease' EquivalentTo http://www.ebi.ac.uk/efo/EFO_0005809
http://purl.obolibrary.org/obo/MONDO_0025512 EquivalentTo http://www.ebi.ac.uk/efo/EFO_0005809
http://purl.obolibrary.org/obo/MONDO_0016286
adenoid cystic carcinoma of the cervix uteri
'adenoid cystic carcinoma of the cervix uteri' SubClassOf 'rare cancer of cervix uteri'
'adenoid cystic carcinoma of the cervix uteri' SubClassOf 'cervical carcinoma'
'adenoid cystic carcinoma of the cervix uteri' SubClassOf 'adenocarcinoma of cervix uteri'
http://purl.obolibrary.org/obo/MONDO_0012626
Meckel syndrome, type 4
'Meckel syndrome, type 4' SubClassOf 'Meckel syndrome'
'Meckel syndrome, type 4' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070118 EquivalentTo 'Meckel syndrome, type 4'
http://purl.obolibrary.org/obo/MONDO_0012695
Meckel syndrome, type 5
'Meckel syndrome, type 5' SubClassOf 'Meckel syndrome'
'Meckel syndrome, type 5' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070119 EquivalentTo 'Meckel syndrome, type 5'
http://purl.obolibrary.org/obo/MONDO_0012504
camptodactyly-tall stature-scoliosis-hearing loss syndrome
http://purl.obolibrary.org/obo/DOID_0111160 EquivalentTo 'camptodactyly-tall stature-scoliosis-hearing loss syndrome'
http://purl.obolibrary.org/obo/GARD_0010012 EquivalentTo 'camptodactyly-tall stature-scoliosis-hearing loss syndrome'
'camptodactyly-tall stature-scoliosis-hearing loss syndrome' SubClassOf 'autosomal genetic disease'
http://purl.obolibrary.org/obo/MONDO_0012511
preterm premature rupture of the membranes
http://purl.obolibrary.org/obo/DOID_0111144 EquivalentTo 'preterm premature rupture of the membranes'
'preterm premature rupture of the membranes' SubClassOf 'female reproductive system disease'
http://purl.obolibrary.org/obo/MONDO_0012561
congenital anomalies of kidney and urinary tract 1, susceptibility to
http://purl.obolibrary.org/obo/DOID_0080206 EquivalentTo 'congenital anomalies of kidney and urinary tract 1, susceptibility to'
http://purl.obolibrary.org/obo/MONDO_0012579
autoimmune pulmonary alveolar proteinosis
'autoimmune pulmonary alveolar proteinosis' SubClassOf 'has modifier' some 'acquired'
'autoimmune pulmonary alveolar proteinosis' EquivalentTo 'pulmonary alveolar proteinosis' and ('has modifier' some 'acquired')
'autoimmune pulmonary alveolar proteinosis' EquivalentTo 'pulmonary alveolar proteinosis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune pulmonary alveolar proteinosis' SubClassOf 'rare immune disease'
'autoimmune pulmonary alveolar proteinosis' SubClassOf 'hypersensitivity reaction type II disease'
http://purl.obolibrary.org/obo/MONDO_0012407
Pyridoxal phosphate-responsive seizures
'Pyridoxal phosphate-responsive seizures' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/MONDO_0012455
Kleefstra syndrome
'Kleefstra syndrome' EquivalentTo http://purl.obolibrary.org/obo/OMIM_610253
http://purl.obolibrary.org/obo/MONDO_0002915
childhood infratentorial neoplasm
'childhood infratentorial neoplasm' SubClassOf 'brainstem cancer'
'childhood infratentorial neoplasm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037736
'childhood infratentorial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037736 and ('has modifier' some http://purl.obolibrary.org/obo/HP_0011463)
'childhood infratentorial neoplasm' SubClassOf 'childhood neoplasm'
http://purl.obolibrary.org/obo/MONDO_0002914
childhood brain stem neoplasm
'childhood brain stem neoplasm' SubClassOf 'brainstem cancer'
http://purl.obolibrary.org/obo/MONDO_0002920
malignant ovarian Brenner tumor
'malignant ovarian Brenner tumor' SubClassOf 'ovarian cancer'
'malignant ovarian Brenner tumor' SubClassOf 'malignant epithelial tumor of ovary'
http://purl.obolibrary.org/obo/MONDO_0012360
CHNG3
http://purl.obolibrary.org/obo/DOID_0070127 EquivalentTo 'CHNG3'
http://purl.obolibrary.org/obo/MONDO_0012166
ataxia, sensory, 1, autosomal dominant
'ataxia, sensory, 1, autosomal dominant' SubClassOf 'rare genetic developmental defect during embryogenesis'
http://purl.obolibrary.org/obo/DOID_0111170 EquivalentTo 'ataxia, sensory, 1, autosomal dominant'
'ataxia, sensory, 1, autosomal dominant' SubClassOf 'rare genetic movement disorder'
'ataxia, sensory, 1, autosomal dominant' SubClassOf 'hereditary ataxia'
http://purl.obolibrary.org/obo/MONDO_0002812
infectious otitis interna
'infectious otitis interna' SubClassOf 'post-infectious disorder'
http://purl.obolibrary.org/obo/MONDO_0002852
mediastinum sarcoma
'mediastinum sarcoma' SubClassOf 'mediastinal cancer'
'mediastinum sarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037743
http://purl.obolibrary.org/obo/MONDO_0002855
ectomesenchymoma
'ectomesenchymoma' SubClassOf 'central nervous system mesenchymal non-meningothelial tumor'
'ectomesenchymoma' SubClassOf 'sarcoma'
'ectomesenchymoma' SubClassOf 'nervous system cancer'
http://purl.obolibrary.org/obo/MONDO_0002872
trophoblastic neoplasm
'trophoblastic neoplasm' SubClassOf 'germ cell and embryonal cancer'
'trophoblastic neoplasm' SubClassOf 'germ cell and embryonal cancer'
http://purl.obolibrary.org/obo/MONDO_0002892
skull base chordoma
'skull base chordoma' SubClassOf 'rare head and neck tumor'
http://purl.obolibrary.org/obo/MONDO_0012054
schizophrenia 12
'schizophrenia 12' SubClassOf 'schizophrenia (disease)'
'schizophrenia 12' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070088 EquivalentTo 'schizophrenia 12'
http://purl.obolibrary.org/obo/MONDO_0012081
15q11q13 microduplication syndrome
'15q11q13 microduplication syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0012092
hereditary sensory and autonomic neuropathy type 5
http://purl.obolibrary.org/obo/DOID_0070145 EquivalentTo 'hereditary sensory and autonomic neuropathy type 5'
http://purl.obolibrary.org/obo/SCTID_89723004
'chronic tympanitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_89723004
http://purl.obolibrary.org/obo/MONDO_0001227ub EquivalentTo http://purl.obolibrary.org/obo/SCTID_89723004
http://purl.obolibrary.org/obo/MONDO_0002732
lung benign neoplasm
'lung benign neoplasm' SubClassOf 'thoracic benign neoplasm'
'lung benign neoplasm' SubClassOf 'lung neoplasm'
'lung benign neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4454
'lung benign neoplasm' SubClassOf 'thoracic benign neoplasm'
'lung benign neoplasm' SubClassOf 'lung neoplasm'
http://purl.obolibrary.org/obo/MONDO_0012105
Wegener's granulomatosis
'Wegener's granulomatosis' SubClassOf 'autoimmune disease of peripheral nervous system'
'Wegener's granulomatosis' SubClassOf 'autoimmune disease of central nervous system'
'Wegener's granulomatosis' SubClassOf 'autoimmune disease of cardiovascular system'
'Wegener's granulomatosis' SubClassOf 'central nervous system vasculitis'
'Wegener's granulomatosis' SubClassOf 'central nervous system vasculitis'
http://purl.obolibrary.org/obo/MONDO_0012104
partial acquired lipodystrophy
'partial acquired lipodystrophy' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0027767 and ('has modifier' some 'acquired')
'partial acquired lipodystrophy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0027767
http://purl.obolibrary.org/obo/MONDO_0002797
childhood medulloblastoma
'childhood medulloblastoma' SubClassOf 'brain stem medulloblastoma'
'childhood medulloblastoma' SubClassOf 'childhood brain stem neoplasm'
'childhood medulloblastoma' SubClassOf 'medulloblastoma'
http://purl.obolibrary.org/obo/MONDO_0002599
teratocarcinoma
'teratocarcinoma' SubClassOf 'germ cell and embryonal cancer'
'teratocarcinoma' SubClassOf 'mixed germ cell tumor'
'teratocarcinoma' SubClassOf 'germ cell and embryonal cancer'
'teratocarcinoma' SubClassOf 'mixed germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0002600
mixed germ cell cancer
'mixed germ cell cancer' SubClassOf 'cancer'
http://purl.obolibrary.org/obo/DOID_3306 EquivalentTo 'mixed germ cell cancer'
'mixed germ cell cancer' SubClassOf 'germ cell tumor'
'mixed germ cell cancer' EquivalentTo 'germ cell tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
http://purl.obolibrary.org/obo/MONDO_0002601
teratoma
'teratoma' SubClassOf 'nongerminomatous germ cell tumor'
'teratoma' SubClassOf 'germ cell and embryonal cancer'
http://purl.obolibrary.org/obo/MONDO_0002623
pediatric osteosarcoma
'pediatric osteosarcoma' SubClassOf 'childhood malignant neoplasm'
'pediatric osteosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0002678
pediatric fibrosarcoma
'pediatric fibrosarcoma' SubClassOf 'childhood malignant neoplasm'
'pediatric fibrosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0002680
chronic wasting disease
'chronic wasting disease' SubClassOf 'non-human animal disease'
http://purl.obolibrary.org/obo/MONDO_0002460
lacrimal system cancer
'lacrimal system cancer' EquivalentTo 'cancer' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001750)
'lacrimal system cancer' SubClassOf 'lacrimal apparatus disease'
http://purl.obolibrary.org/obo/MONDO_0002489
malignant breast phyllodes tumor
'malignant breast phyllodes tumor' SubClassOf 'malignant mixed neoplasm'
'malignant breast phyllodes tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037003
http://purl.obolibrary.org/obo/MONDO_0002510
germ cell and embryonal cancer
http://purl.obolibrary.org/obo/MESH_D009373 EquivalentTo 'germ cell and embryonal cancer'
http://purl.obolibrary.org/obo/MONDO_0002540
childhood oligodendroglioma
'childhood oligodendroglioma' SubClassOf 'childhood malignant neoplasm'
'childhood oligodendroglioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0002571
central nervous system lymphoma
'central nervous system lymphoma' SubClassOf 'central nervous system cancer'
http://purl.obolibrary.org/obo/MONDO_0007291
familial cerebral cavernous malformation
'familial cerebral cavernous malformation' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0007297
ADan amyloidosis
'ADan amyloidosis' SubClassOf 'cerebral amyloid angiopathy'
'ADan amyloidosis' SubClassOf 'cerebral amyloid angiopathy'
http://purl.obolibrary.org/obo/DOID_0070030 EquivalentTo 'ADan amyloidosis'
http://purl.obolibrary.org/obo/MONDO_0007113
Angelman syndrome
'Angelman syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'Angelman syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0007154
arteriovenous malformations of the brain
'arteriovenous malformations of the brain' SubClassOf 'nervous system benign neoplasm'
'arteriovenous malformations of the brain' SubClassOf 'rare genetic epilepsy'
'arteriovenous malformations of the brain' SubClassOf 'intracranial hemangioma'
http://purl.obolibrary.org/obo/MONDO_0007179
hypersensitivity reaction type II disease
'hypersensitivity reaction type II disease' EquivalentTo http://www.ebi.ac.uk/efo/EFO_0005809
'hypersensitivity reaction type II disease' EquivalentTo 'immune system disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'hypersensitivity reaction type II disease' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445
'hypersensitivity reaction type II disease' EquivalentTo 'disease' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'hypersensitivity reaction type II disease' EquivalentTo http://purl.obolibrary.org/obo/OBI_1110054
'hypersensitivity reaction type II disease' SubClassOf 'disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960
'allergic disease' DisjointWith 'hypersensitivity reaction type II disease'
http://purl.obolibrary.org/obo/MONDO_0007006
ulnar neuropathy
'ulnar neuropathy' SubClassOf 'disorder of anatomical region'
'ulnar neuropathy' EquivalentTo 'mononeuropathy' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001494)
'ulnar neuropathy' SubClassOf 'brachial plexus neuropathy'
'ulnar neuropathy' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0001494
http://purl.obolibrary.org/obo/MONDO_0007004
hypersensitivity reaction type III disease
'hypersensitivity reaction type III disease' EquivalentTo 'immune system disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0001802)
'hypersensitivity reaction type III disease' SubClassOf 'hypersensitivity reaction disease'
'hypersensitivity reaction type III disease' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C114346
'hypersensitivity reaction type III disease' SubClassOf 'hypersensitivity reaction type II disease'
'hypersensitivity reaction type III disease' EquivalentTo 'disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0001802)
http://purl.obolibrary.org/obo/MONDO_0007098
ACys amyloidosis
'ACys amyloidosis' SubClassOf 'cerebral amyloid angiopathy'
http://purl.obolibrary.org/obo/DOID_0070027 EquivalentTo 'ACys amyloidosis'
'ACys amyloidosis' SubClassOf 'cerebral amyloid angiopathy'
http://purl.obolibrary.org/obo/MONDO_0022518
autoimmune inner ear disease
'autoimmune inner ear disease' EquivalentTo 'inner ear disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune inner ear disease' EquivalentTo 'inner ear disease' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0022519
autoimmune myocarditis
'autoimmune myocarditis' SubClassOf 'disease disrupting biological or physiological process'
'autoimmune myocarditis' EquivalentTo 'myocarditis' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune myocarditis' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445
'autoimmune myocarditis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0030701
'autoimmune myocarditis' EquivalentTo 'myocarditis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0012946
mental retardation, autosomal dominant 3
'mental retardation, autosomal dominant 3' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 3' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070033 EquivalentTo 'mental retardation, autosomal dominant 3'
http://purl.obolibrary.org/obo/MONDO_0012947
mental retardation, autosomal dominant 4
'mental retardation, autosomal dominant 4' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070034 EquivalentTo 'mental retardation, autosomal dominant 4'
'mental retardation, autosomal dominant 4' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0012960
mental retardation, autosomal dominant 5
'mental retardation, autosomal dominant 5' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 5' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070035 EquivalentTo 'mental retardation, autosomal dominant 5'
http://purl.obolibrary.org/obo/MONDO_0012994
Dopa-responsive dystonia due to sepiapterin reductase deficiency
http://purl.obolibrary.org/obo/DOID_0111168 EquivalentTo 'Dopa-responsive dystonia due to sepiapterin reductase deficiency'
http://purl.obolibrary.org/obo/MONDO_0012833
Crouzon syndrome-acanthosis nigricans syndrome
http://purl.obolibrary.org/obo/DOID_0111161 EquivalentTo 'Crouzon syndrome-acanthosis nigricans syndrome'
'Crouzon syndrome-acanthosis nigricans syndrome' SubClassOf 'autosomal dominant disease'
http://purl.obolibrary.org/obo/MONDO_0012848
Meckel syndrome, type 6
'Meckel syndrome, type 6' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070120 EquivalentTo 'Meckel syndrome, type 6'
'Meckel syndrome, type 6' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/MONDO_0012869
mental retardation, autosomal dominant 22
'mental retardation, autosomal dominant 22' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 22' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070052 EquivalentTo 'mental retardation, autosomal dominant 22'
http://purl.obolibrary.org/obo/MONDO_0012879
schizophrenia 14
'schizophrenia 14' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070090 EquivalentTo 'schizophrenia 14'
'schizophrenia 14' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0012774
chromosome 15q13.3 microdeletion syndrome
'chromosome 15q13.3 microdeletion syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'chromosome 15q13.3 microdeletion syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0017410
porencephaly
'porencephaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/DOID_7192
http://purl.obolibrary.org/obo/DOID_7192 EquivalentTo 'hereditary conventional renal cell carcinoma'
http://purl.obolibrary.org/obo/DOID_7192 EquivalentTo 'hereditary clear cell renal cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0007925
chromosome 5q deletion syndrome
'chromosome 5q deletion syndrome' SubClassOf 'rare genetic inherited tumor'
'chromosome 5q deletion syndrome' SubClassOf 'rare genetic bone disease'
'chromosome 5q deletion syndrome' SubClassOf 'inherited syndrome with bone tumors as a major feature'
http://purl.obolibrary.org/obo/MONDO_0007969
Melkersson-Rosenthal syndrome
'Melkersson-Rosenthal syndrome' SubClassOf 'rare genetic immune disease'
'Melkersson-Rosenthal syndrome' SubClassOf 'gastrointestinal allergy'
http://purl.obolibrary.org/obo/MONDO_0007974
mental retardation, autosomal dominant 1
'mental retardation, autosomal dominant 1' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 1' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070031 EquivalentTo 'mental retardation, autosomal dominant 1'
http://purl.obolibrary.org/obo/MONDO_0017364
POEMS syndrome
'POEMS syndrome' SubClassOf 'rare nervous system tumor'
'POEMS syndrome' SubClassOf 'peripheral nervous system neoplasm'
'POEMS syndrome' SubClassOf 'autoimmune disease of blood'
'POEMS syndrome' SubClassOf 'autoimmune neuropathy'
'POEMS syndrome' SubClassOf 'central nervous system lymphoma'
'POEMS syndrome' SubClassOf 'peripheral nervous system cancer'
http://purl.obolibrary.org/obo/MONDO_0007845
Kaposi sarcoma, susceptibility to
'Kaposi sarcoma, susceptibility to' SubClassOf 'multicentric Castleman disease'
http://purl.obolibrary.org/obo/MONDO_0007858
palmoplantar keratoderma, punctate type 1A
http://purl.obolibrary.org/obo/DOID_0080214 EquivalentTo 'palmoplantar keratoderma, punctate type 1A'
http://purl.obolibrary.org/obo/MONDO_0017278
autoimmune polyendocrinopathy
'autoimmune polyendocrinopathy' EquivalentTo 'polyendocrinopathy' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune polyendocrinopathy' EquivalentTo 'polyendocrinopathy' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0007741
congenital hydronephrosis
'congenital hydronephrosis' EquivalentTo http://www.orpha.net/ORDO/Orphanet_2190
'congenital hydronephrosis' SubClassOf 'bilateral multicystic dysplastic kidney'
'congenital hydronephrosis' EquivalentTo http://purl.obolibrary.org/obo/OMIM_143400
http://purl.obolibrary.org/obo/MONDO_0007758
epidermolytic palmoplantar keratoderma
http://purl.obolibrary.org/obo/DOID_0080223 EquivalentTo 'epidermolytic palmoplantar keratoderma'
http://purl.obolibrary.org/obo/MONDO_0007785
hyperthyroxinemia, Dystransthyretinemic
'hyperthyroxinemia, Dystransthyretinemic' SubClassOf 'hyperthyroxinemia'
http://purl.obolibrary.org/obo/DOID_0080219 EquivalentTo 'hyperthyroxinemia, Dystransthyretinemic'
'hyperthyroxinemia, Dystransthyretinemic' SubClassOf 'hyperthyroxinemia'
http://purl.obolibrary.org/obo/MONDO_0017169
multiple endocrine neoplasia
'multiple endocrine neoplasia' SubClassOf 'rare genetic inherited tumor'
'multiple endocrine neoplasia' SubClassOf 'rare genetic endocrine disease'
http://purl.obolibrary.org/obo/MONDO_0007672
glomuvenous malformation
'glomuvenous malformation' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0017043
congenital mesoblastic nephroma
'congenital mesoblastic nephroma' SubClassOf 'childhood malignant neoplasm'
'congenital mesoblastic nephroma' SubClassOf 'childhood kidney neoplasm'
'congenital mesoblastic nephroma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036511
'congenital mesoblastic nephroma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0017094
cerebral cortical dysplasia
'cerebral cortical dysplasia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/MONDO_0007514
ectopia lentis 1, isolated, autosomal dominant
http://purl.obolibrary.org/obo/DOID_0111150 EquivalentTo 'ectopia lentis 1, isolated, autosomal dominant'
http://purl.obolibrary.org/obo/MONDO_0007549
generalized dominant dystrophic epidermolysis bullosa
'generalized dominant dystrophic epidermolysis bullosa' SubClassOf 'epidermolysis bullosa dystrophica'
'generalized dominant dystrophic epidermolysis bullosa' SubClassOf 'epidermolysis bullosa dystrophica'
http://purl.obolibrary.org/obo/DOID_0080224 EquivalentTo 'generalized dominant dystrophic epidermolysis bullosa'
http://purl.obolibrary.org/obo/MONDO_0007411
cutis laxa, autosomal dominant 1
http://purl.obolibrary.org/obo/DOID_0070130 EquivalentTo 'cutis laxa, autosomal dominant 1'
http://purl.obolibrary.org/obo/MONDO_0007447
autosomal dominant vibratory urticaria
'autosomal dominant vibratory urticaria' SubClassOf 'rare genetic immune disease'
http://purl.obolibrary.org/obo/MONDO_0007440
MAFD1
'MAFD1' SubClassOf 'bipolar disorder'
http://purl.obolibrary.org/obo/DOID_0080220 EquivalentTo 'MAFD1'
'MAFD1' SubClassOf 'bipolar I disorder'
http://purl.obolibrary.org/obo/MONDO_0007485
dyskeratosis congenita, autosomal dominant 1
'dyskeratosis congenita, autosomal dominant 1' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070014 EquivalentTo 'dyskeratosis congenita, autosomal dominant 1'
'dyskeratosis congenita, autosomal dominant 1' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/MONDO_0013056
epileptic encephalopathy with global cerebral demyelination
'epileptic encephalopathy with global cerebral demyelination' SubClassOf 'neonatal epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0013051
autosomal recessive cutis laxa type 2B
http://purl.obolibrary.org/obo/DOID_0070137 EquivalentTo 'autosomal recessive cutis laxa type 2B'
http://purl.obolibrary.org/obo/MONDO_0013089
SCZD13
'SCZD13' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070089 EquivalentTo 'SCZD13'
'SCZD13' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0003710
ovarian mixed germ cell neoplasm
'ovarian mixed germ cell neoplasm' SubClassOf 'malignant non-dysgerminomatous germ cell tumor of ovary'
'ovarian mixed germ cell neoplasm' SubClassOf 'mixed germ cell tumor'
'ovarian mixed germ cell neoplasm' SubClassOf 'mixed germ cell tumor'
'ovarian mixed germ cell neoplasm' SubClassOf 'ovarian primitive germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0003758
childhood testicular germ cell tumor
'childhood testicular germ cell tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037250
http://purl.obolibrary.org/obo/MONDO_0003787
childhood testicular mixed germ cell tumor
'childhood testicular mixed germ cell tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003788
childhood embryonal testis carcinoma
'childhood embryonal testis carcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003786
childhood testicular choriocarcinoma
'childhood testicular choriocarcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003578
extragonadal nonseminomatous germ cell tumor
'extragonadal nonseminomatous germ cell tumor' SubClassOf 'nongerminomatous germ cell tumor'
'extragonadal nonseminomatous germ cell tumor' SubClassOf 'extragonadal non-dysgerminomatous germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0003587
pediatric liposarcoma
'pediatric liposarcoma' SubClassOf 'childhood malignant neoplasm'
'pediatric liposarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003596
spindle cell liposarcoma
'spindle cell liposarcoma' SubClassOf 'atypical lipomatous tumor'
http://purl.obolibrary.org/obo/MONDO_0003597
mixed-type liposarcoma
'mixed-type liposarcoma' SubClassOf 'liposarcoma'
http://purl.obolibrary.org/obo/DOID_5709 EquivalentTo 'mixed-type liposarcoma'
http://purl.obolibrary.org/obo/MONDO_0003595
sclerosing liposarcoma
'sclerosing liposarcoma' SubClassOf 'atypical lipomatous tumor'
'sclerosing liposarcoma' SubClassOf 'well-differentiated liposarcoma'
http://purl.obolibrary.org/obo/OMIM_263200
'autosomal recessive polycystic kidney disease' EquivalentTo http://purl.obolibrary.org/obo/OMIM_263200
http://purl.obolibrary.org/obo/MONDO_0033004 EquivalentTo http://purl.obolibrary.org/obo/OMIM_263200
http://purl.obolibrary.org/obo/MONDO_0003603
non-functioning pituitary gland neoplasm
'non-functioning pituitary gland neoplasm' SubClassOf 'pituitary gland disease'
'non-functioning pituitary gland neoplasm' SubClassOf 'brain neoplasm'
'non-functioning pituitary gland neoplasm' SubClassOf 'pituitary tumor'
http://purl.obolibrary.org/obo/MONDO_0003604
functioning pituitary gland neoplasm
'functioning pituitary gland neoplasm' SubClassOf 'brain neoplasm'
'functioning pituitary gland neoplasm' SubClassOf 'pituitary gland disease'
'functioning pituitary gland neoplasm' SubClassOf 'pituitary tumor'
'functioning pituitary gland neoplasm' EquivalentTo http://purl.obolibrary.org/obo/SCTID_448148000
http://purl.obolibrary.org/obo/MONDO_0003637
lung clear cell-sugar-tumor
'lung clear cell-sugar-tumor' SubClassOf 'benign perivascular tumor'
'lung clear cell-sugar-tumor' SubClassOf 'neoplasm with perivascular epithelioid cell differentiation'
http://purl.obolibrary.org/obo/MONDO_0003646
rectum neuroendocrine neoplasm
'rectum neuroendocrine neoplasm' SubClassOf 'rectal cancer'
'rectum neuroendocrine neoplasm' SubClassOf 'colorectal carcinoma'
'rectum neuroendocrine neoplasm' SubClassOf 'neuroendocrine carcinoma'
http://purl.obolibrary.org/obo/MONDO_0003641
central nervous system hematopoietic neoplasm
'central nervous system hematopoietic neoplasm' SubClassOf 'central nervous system cancer'
'central nervous system hematopoietic neoplasm' SubClassOf 'central nervous system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0003659
pediatric lymphoma
'pediatric lymphoma' SubClassOf 'childhood malignant neoplasm'
'pediatric lymphoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003430
prolactin producing pituitary tumor
'prolactin producing pituitary tumor' SubClassOf 'endocrine gland neoplasm'
'prolactin producing pituitary tumor' SubClassOf 'brain neoplasm'
'prolactin producing pituitary tumor' SubClassOf 'pituitary gland disease'
'prolactin producing pituitary tumor' SubClassOf 'pituitary tumor'
http://purl.obolibrary.org/obo/MONDO_0003504
anal canal neuroendocrine neoplasm
'anal canal neuroendocrine neoplasm' SubClassOf 'neuroendocrine carcinoma'
http://purl.obolibrary.org/obo/MONDO_0003512
mediastinal mesenchymal tumor
'mediastinal mesenchymal tumor' SubClassOf 'mediastinal cancer'
'mediastinal mesenchymal tumor' SubClassOf 'neoplasm of mediastinum'
'mediastinal mesenchymal tumor' EquivalentTo 'soft tissue neoplasm' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0003728)
http://purl.obolibrary.org/obo/MONDO_0003514
malignant teratoma
'malignant teratoma' SubClassOf 'mixed germ cell cancer'
'malignant teratoma' SubClassOf 'malignant germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0003314
endometrioid stromal and related neoplasms of the vagina
'endometrioid stromal and related neoplasms of the vagina' SubClassOf 'vaginal cancer'
'endometrioid stromal and related neoplasms of the vagina' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037742 and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000996)
'endometrioid stromal and related neoplasms of the vagina' SubClassOf 'vaginal neoplasm'
'endometrioid stromal and related neoplasms of the vagina' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037742
http://purl.obolibrary.org/obo/MONDO_0003311
endometrial stromal tumor
'endometrial stromal tumor' SubClassOf 'endometrial cancer'
'endometrial stromal tumor' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002337)
'endometrial stromal tumor' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0002337
'endometrial stromal tumor' SubClassOf 'endometrium neoplasm'
http://purl.obolibrary.org/obo/MONDO_0003312
ovarian endometrioid stromal and related neoplasms
'ovarian endometrioid stromal and related neoplasms' SubClassOf 'ovarian sarcoma'
'ovarian endometrioid stromal and related neoplasms' SubClassOf 'ovarian neoplasm'
'ovarian endometrioid stromal and related neoplasms' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037742 and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000992)
'ovarian endometrioid stromal and related neoplasms' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037742
http://purl.obolibrary.org/obo/MONDO_0003323
cervical wilms' tumor
http://purl.obolibrary.org/obo/DOID_5190 EquivalentTo 'cervical wilms' tumor'
'cervical wilms' tumor' SubClassOf 'cervical carcinosarcoma'
http://linkedlifedata.com/resource/umls/id/C1516437 EquivalentTo 'cervical wilms' tumor'
http://purl.obolibrary.org/obo/MONDO_0017979
autoimmune lymphoproliferative syndrome
'autoimmune lymphoproliferative syndrome' EquivalentTo 'lymphoproliferative syndrome' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0003349
central nervous system leiomyosarcoma
'central nervous system leiomyosarcoma' SubClassOf 'central nervous system mesenchymal non-meningothelial tumor'
'central nervous system leiomyosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037740
http://purl.obolibrary.org/obo/MONDO_0017986
disorder of plasmalogens biosynthesis
'disorder of plasmalogens biosynthesis' SubClassOf 'inherited lipid metabolism disorder'
'disorder of plasmalogens biosynthesis' SubClassOf 'rare dyslipidemia'
http://purl.obolibrary.org/obo/MONDO_0003392
fallopian tube germ cell cancer
'fallopian tube germ cell cancer' SubClassOf 'mixed germ cell cancer'
'fallopian tube germ cell cancer' SubClassOf 'malignant germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0003400
childhood endodermal sinus tumor
'childhood endodermal sinus tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003419
Bartholin's gland adenoma
'Bartholin's gland adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0003424
oncocytic adenoma
'oncocytic adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0003422
lung adenoma
'lung adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0003423
middle ear adenoma
'middle ear adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0017851
erythrokeratodermia variabilis
'erythrokeratodermia variabilis' EquivalentTo http://purl.obolibrary.org/obo/OMIM_133200
'erythrokeratodermia variabilis' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_133200
http://purl.obolibrary.org/obo/MONDO_0003235
optic nerve glioma
'optic nerve glioma' SubClassOf 'rare head and neck tumor'
http://purl.obolibrary.org/obo/MONDO_0003244
central nervous system mesenchymal non-meningothelial tumor
'central nervous system mesenchymal non-meningothelial tumor' SubClassOf 'central nervous system cancer'
http://purl.obolibrary.org/obo/MONDO_0003245
aflatoxins-related hepatocellular carcinoma
'aflatoxins-related hepatocellular carcinoma' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/ECTO_0001108
'aflatoxins-related hepatocellular carcinoma' EquivalentTo 'hepatocellular carcinoma' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/ECTO_0001108)
http://purl.obolibrary.org/obo/MONDO_0003255
mediastinal granular cell myoblastoma
'mediastinal granular cell myoblastoma' SubClassOf 'granular cell cancer'
'mediastinal granular cell myoblastoma' SubClassOf 'mediastinal cancer'
'mediastinal granular cell myoblastoma' SubClassOf 'granular cell tumor'
http://purl.obolibrary.org/obo/MONDO_0017893
inherited acute myeloid leukemia
'inherited acute myeloid leukemia' SubClassOf 'rare genetic bone disease'
'inherited acute myeloid leukemia' SubClassOf 'rare genetic inherited tumor'
'inherited acute myeloid leukemia' SubClassOf 'inherited syndrome with bone tumors as a major feature'
http://purl.obolibrary.org/obo/MONDO_0003263
childhood cerebellar neoplasm
'childhood cerebellar neoplasm' SubClassOf 'cancer of cerebellum'
'childhood cerebellar neoplasm' SubClassOf 'cerebellar neoplasm'
http://purl.obolibrary.org/obo/MONDO_0017768
reflex epilepsy
'reflex epilepsy' SubClassOf 'childhood electroclinical syndrome'
'reflex epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100036
http://purl.obolibrary.org/obo/MONDO_0017799
Meigs syndrome
'Meigs syndrome' SubClassOf 'has modifier' some 'acquired'
http://purl.obolibrary.org/obo/MONDO_0017795
ameloblastoma
'ameloblastoma' SubClassOf 'epithelial neoplasm'
'ameloblastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0003163
cauda equina intradural extramedullary astrocytoma
'cauda equina intradural extramedullary astrocytoma' SubClassOf 'spinal cord astrocytoma'
'cauda equina intradural extramedullary astrocytoma' SubClassOf 'astrocytoma (excluding glioblastoma)'
http://purl.obolibrary.org/obo/MONDO_0003164
cauda equina neoplasm
'cauda equina neoplasm' SubClassOf 'spinal cord cancer'
'cauda equina neoplasm' SubClassOf 'peripheral nervous system cancer'
http://purl.obolibrary.org/obo/MONDO_0003177
prostate adenoid cystic carcinoma
'prostate adenoid cystic carcinoma' SubClassOf 'prostate carcinoma'
'prostate adenoid cystic carcinoma' SubClassOf 'prostate adenocarcinoma'
http://purl.obolibrary.org/obo/MONDO_0003170
gliofibroma
'gliofibroma' SubClassOf 'astrocytoma (excluding glioblastoma)'
'gliofibroma' SubClassOf 'astrocytic tumor'
http://purl.obolibrary.org/obo/MONDO_0003185
adenoid cystic breast carcinoma
'adenoid cystic breast carcinoma' SubClassOf 'breast adenocarcinoma'
http://purl.obolibrary.org/obo/MONDO_0003186
esophageal adenoid cystic carcinoma
'esophageal adenoid cystic carcinoma' SubClassOf 'carcinoma of esophagus'
'esophageal adenoid cystic carcinoma' SubClassOf 'esophageal adenocarcinoma'
http://purl.obolibrary.org/obo/MONDO_0003187
Bartholin's gland adenoid cystic carcinoma
'Bartholin's gland adenoid cystic carcinoma' SubClassOf 'Bartholin gland carcinoma'
'Bartholin's gland adenoid cystic carcinoma' SubClassOf 'Bartholin's gland adenocarcinoma'
http://purl.obolibrary.org/obo/MONDO_0003181
lung adenoid cystic carcinoma
'lung adenoid cystic carcinoma' SubClassOf 'lung carcinoma'
'lung adenoid cystic carcinoma' SubClassOf 'lung adenocarcinoma'
http://purl.obolibrary.org/obo/MONDO_0017807
growing teratoma syndrome
'growing teratoma syndrome' SubClassOf 'has modifier' some 'acquired'
http://purl.obolibrary.org/obo/MONDO_0017814
primary bone lymphoma
'primary bone lymphoma' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0017611
pituitary tumor
'pituitary tumor' SubClassOf 'brain neoplasm'
'pituitary tumor' EquivalentTo 'sella turcica neoplasm' and 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000007)
'pituitary tumor' SubClassOf 'pituitary gland disease'
'pituitary tumor' SubClassOf 'hypothalamic neoplasm'
'pituitary tumor' SubClassOf 'pituitary gland disease'
'pituitary tumor' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000007)
'pituitary tumor' EquivalentTo http://purl.obolibrary.org/obo/SCTID_127024001
http://purl.obolibrary.org/obo/MONDO_0003007
childhood kidney cell carcinoma
'childhood kidney cell carcinoma' SubClassOf 'childhood kidney neoplasm'
'childhood kidney cell carcinoma' SubClassOf 'childhood malignant neoplasm'
'childhood kidney cell carcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
'childhood kidney cell carcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036511
http://purl.obolibrary.org/obo/MONDO_0003017
malignant peritoneal solitary fibrous tumor
'malignant peritoneal solitary fibrous tumor' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037737 and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
'malignant peritoneal solitary fibrous tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037737
'malignant peritoneal solitary fibrous tumor' SubClassOf 'connective tissue cancer'
http://purl.obolibrary.org/obo/MONDO_0017655
progressive epilepsy and/or ataxia with myoclonus as a major feature
'progressive epilepsy and/or ataxia with myoclonus as a major feature' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100036
'progressive epilepsy and/or ataxia with myoclonus as a major feature' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0003022
pediatric angiosarcoma
'pediatric angiosarcoma' SubClassOf 'childhood malignant neoplasm'
'pediatric angiosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0017569
de Barsy syndrome
'de Barsy syndrome' SubClassOf 'cutis laxa'
'de Barsy syndrome' SubClassOf 'cutis laxa'
http://purl.obolibrary.org/obo/DOID_0070143 EquivalentTo 'de Barsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0013922
microcephalic primordial dwarfism, Dauber type
'microcephalic primordial dwarfism, Dauber type' SubClassOf 'Seckel syndrome'
'microcephalic primordial dwarfism, Dauber type' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070011 EquivalentTo 'microcephalic primordial dwarfism, Dauber type'
http://purl.obolibrary.org/obo/MONDO_0013804
mental retardation, autosomal dominant 12
http://purl.obolibrary.org/obo/DOID_0070042 EquivalentTo 'mental retardation, autosomal dominant 12'
http://purl.obolibrary.org/obo/MONDO_0013805
mental retardation, autosomal dominant 13
'mental retardation, autosomal dominant 13' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 13' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070043 EquivalentTo 'mental retardation, autosomal dominant 13'
http://purl.obolibrary.org/obo/MONDO_0013819
mental retardation, autosomal dominant 14
http://purl.obolibrary.org/obo/DOID_0070044 EquivalentTo 'mental retardation, autosomal dominant 14'
http://purl.obolibrary.org/obo/MONDO_0013821
mental retardation, autosomal dominant 16
http://purl.obolibrary.org/obo/DOID_0070046 EquivalentTo 'mental retardation, autosomal dominant 16'
http://purl.obolibrary.org/obo/MONDO_0013820
mental retardation, autosomal dominant 15
http://purl.obolibrary.org/obo/DOID_0070045 EquivalentTo 'mental retardation, autosomal dominant 15'
http://purl.obolibrary.org/obo/MONDO_0013839
hereditary sensory and autonomic neuropathy type 6
http://purl.obolibrary.org/obo/DOID_0070151 EquivalentTo 'hereditary sensory and autonomic neuropathy type 6'
http://purl.obolibrary.org/obo/MONDO_0013871
Seckel syndrome 6
'Seckel syndrome 6' SubClassOf 'Seckel syndrome'
'Seckel syndrome 6' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070006 EquivalentTo 'Seckel syndrome 6'
http://purl.obolibrary.org/obo/MONDO_0013757
hypothyroidism, congenital, Nongoitrous, 6
http://purl.obolibrary.org/obo/DOID_0070128 EquivalentTo 'hypothyroidism, congenital, Nongoitrous, 6'
http://purl.obolibrary.org/obo/MONDO_0013755
PYCR1-related de Barsy syndrome
http://purl.obolibrary.org/obo/DOID_0070138 EquivalentTo 'PYCR1-related de Barsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0013754
cutis laxa, autosomal recessive, type 1B
http://purl.obolibrary.org/obo/DOID_0070133 EquivalentTo 'cutis laxa, autosomal recessive, type 1B'
http://purl.obolibrary.org/obo/MONDO_0013766
familial cold autoinflammatory syndrome 3
'familial cold autoinflammatory syndrome 3' SubClassOf 'rare urticaria'
'familial cold autoinflammatory syndrome 3' SubClassOf 'autoimmune disease with skin involvement'
'familial cold autoinflammatory syndrome 3' SubClassOf 'primary immunodeficiency due to a defect in adaptive immunity'
'familial cold autoinflammatory syndrome 3' SubClassOf http://purl.obolibrary.org/obo/MONDO_0025513
http://purl.obolibrary.org/obo/DOID_3306
http://purl.obolibrary.org/obo/DOID_3306 EquivalentTo 'mixed germ cell cancer'
http://purl.obolibrary.org/obo/DOID_3306 EquivalentTo 'mixed germ cell tumor'
http://purl.obolibrary.org/obo/GARD_0006240
http://purl.obolibrary.org/obo/GARD_0006240 EquivalentTo 'atypical hemolytic-uremic syndrome'
http://purl.obolibrary.org/obo/MONDO_0013634
neuropathy, hereditary sensory, type 2C
http://purl.obolibrary.org/obo/DOID_0070147 EquivalentTo 'neuropathy, hereditary sensory, type 2C'
http://purl.obolibrary.org/obo/MONDO_0013658
mental retardation, autosomal dominant 11
'mental retardation, autosomal dominant 11' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 11' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070041 EquivalentTo 'mental retardation, autosomal dominant 11'
http://purl.obolibrary.org/obo/MONDO_0013656
mental retardation, autosomal dominant 9
'mental retardation, autosomal dominant 9' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 9' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070039 EquivalentTo 'mental retardation, autosomal dominant 9'
http://purl.obolibrary.org/obo/MONDO_0013657
mental retardation, autosomal dominant 10
'mental retardation, autosomal dominant 10' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 10' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070040 EquivalentTo 'mental retardation, autosomal dominant 10'
http://purl.obolibrary.org/obo/MONDO_0013655
mental retardation, autosomal dominant 8
'mental retardation, autosomal dominant 8' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 8' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070038 EquivalentTo 'mental retardation, autosomal dominant 8'
http://purl.obolibrary.org/obo/MONDO_0013472
fatal infantile hypertonic myofibrillar myopathy
http://purl.obolibrary.org/obo/DOID_0080098 EquivalentTo 'fatal infantile hypertonic myofibrillar myopathy'
http://purl.obolibrary.org/obo/DOID_0080309 EquivalentTo 'fatal infantile hypertonic myofibrillar myopathy'
http://purl.obolibrary.org/obo/MONDO_0013482
Meckel syndrome, type 8
'Meckel syndrome, type 8' SubClassOf 'Meckel syndrome'
'Meckel syndrome, type 8' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070122 EquivalentTo 'Meckel syndrome, type 8'
http://purl.obolibrary.org/obo/MONDO_0013498
schizophrenia 15
'schizophrenia 15' SubClassOf 'schizophrenia (disease)'
'schizophrenia 15' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070091 EquivalentTo 'schizophrenia 15'
http://purl.obolibrary.org/obo/MONDO_0013506
schizophrenia 16
'schizophrenia 16' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070092 EquivalentTo 'schizophrenia 16'
'schizophrenia 16' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0013509
mental retardation, autosomal dominant 6
'mental retardation, autosomal dominant 6' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 6' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070036 EquivalentTo 'mental retardation, autosomal dominant 6'
http://purl.obolibrary.org/obo/MONDO_0013519
dyskeratosis congenita, autosomal recessive 2
'dyskeratosis congenita, autosomal recessive 2' SubClassOf 'dyskeratosis congenita'
'dyskeratosis congenita, autosomal recessive 2' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070017 EquivalentTo 'dyskeratosis congenita, autosomal recessive 2'
http://purl.obolibrary.org/obo/MONDO_0013520
dyskeratosis congenita, autosomal recessive 3
'dyskeratosis congenita, autosomal recessive 3' SubClassOf 'dyskeratosis congenita'
'dyskeratosis congenita, autosomal recessive 3' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070019 EquivalentTo 'dyskeratosis congenita, autosomal recessive 3'
http://purl.obolibrary.org/obo/MONDO_0013521
dyskeratosis congenita, autosomal dominant 2
'dyskeratosis congenita, autosomal dominant 2' SubClassOf 'Hoyeraal-Hreidarsson syndrome'
http://purl.obolibrary.org/obo/DOID_0070016 EquivalentTo 'dyskeratosis congenita, autosomal dominant 2'
'dyskeratosis congenita, autosomal dominant 2' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/MONDO_0013522
dyskeratosis congenita, autosomal dominant 3
'dyskeratosis congenita, autosomal dominant 3' SubClassOf 'Hoyeraal-Hreidarsson syndrome'
http://purl.obolibrary.org/obo/DOID_0070018 EquivalentTo 'dyskeratosis congenita, autosomal dominant 3'
'dyskeratosis congenita, autosomal dominant 3' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/MONDO_0013578
DYRK1A-related intellectual disability syndrome
http://purl.obolibrary.org/obo/DOID_0070037 EquivalentTo 'DYRK1A-related intellectual disability syndrome'
http://purl.obolibrary.org/obo/MONDO_0013584
hereditary sensory neuropathy-deafness-dementia syndrome
http://purl.obolibrary.org/obo/DOID_0070158 EquivalentTo 'hereditary sensory neuropathy-deafness-dementia syndrome'
http://purl.obolibrary.org/obo/MONDO_0013581
mental retardation, autosomal dominant 2
'mental retardation, autosomal dominant 2' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070032 EquivalentTo 'mental retardation, autosomal dominant 2'
'mental retardation, autosomal dominant 2' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0013358
Seckel syndrome 4
'Seckel syndrome 4' SubClassOf 'Seckel syndrome'
'Seckel syndrome 4' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070010 EquivalentTo 'Seckel syndrome 4'
http://purl.obolibrary.org/obo/MONDO_0013381
neuropathy, hereditary sensory, type 1D
http://purl.obolibrary.org/obo/DOID_0070156 EquivalentTo 'neuropathy, hereditary sensory, type 1D'
http://purl.obolibrary.org/obo/MONDO_0013443
Seckel syndrome 5
'Seckel syndrome 5' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070012 EquivalentTo 'Seckel syndrome 5'
'Seckel syndrome 5' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/MONDO_0013266
mental retardation, autosomal dominant 20
'mental retardation, autosomal dominant 20' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070050 EquivalentTo 'mental retardation, autosomal dominant 20'
'mental retardation, autosomal dominant 20' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0013280
myxoid liposarcoma
'myxoid liposarcoma' SubClassOf 'leiomyosarcoma'
http://purl.obolibrary.org/obo/DOID_5709 EquivalentTo 'myxoid liposarcoma'
http://purl.obolibrary.org/obo/MONDO_0003924
adrenal cortex adenoma
'adrenal cortex adenoma' SubClassOf 'adrenal cortex disease'
'adrenal cortex adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036591
'adrenal cortex adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0003933
chest wall bone cancer
'chest wall bone cancer' SubClassOf 'chest wall lymphoma'
'chest wall bone cancer' SubClassOf 'malignant neoplasm of chest wall'
http://purl.obolibrary.org/obo/MONDO_0003953
pediatric CNS choriocarcinoma
'pediatric CNS choriocarcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0003988
sternum lymphoma
'sternum lymphoma' SubClassOf 'lymphoma'
'sternum lymphoma' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0003984
internal auditory canal lipoma
'internal auditory canal lipoma' SubClassOf 'auditory system cancer'
'internal auditory canal lipoma' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0011859
'internal auditory canal lipoma' SubClassOf 'benign neoplasm of ear'
'internal auditory canal lipoma' EquivalentTo 'lipoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0011859)
'internal auditory canal lipoma' SubClassOf 'lipoma'
'internal auditory canal lipoma' SubClassOf 'inner ear neoplasm'
http://purl.obolibrary.org/obo/MONDO_0003992
childhood botryoid rhabdomyosarcoma
'childhood botryoid rhabdomyosarcoma' SubClassOf 'childhood malignant neoplasm'
'childhood botryoid rhabdomyosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0013337
neuropathy, hereditary sensory and autonomic, type 1C
http://purl.obolibrary.org/obo/DOID_0070157 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 1C'
http://purl.obolibrary.org/obo/MONDO_0013142
neuropathy, hereditary sensory and autonomic, type 2B
http://purl.obolibrary.org/obo/DOID_0070150 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 2B'
http://purl.obolibrary.org/obo/MONDO_0013170
cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
http://purl.obolibrary.org/obo/DOID_0070139 EquivalentTo 'cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies'
http://purl.obolibrary.org/obo/MONDO_0003806
thyroid hyalinizing trabecular adenoma
'thyroid hyalinizing trabecular adenoma' SubClassOf 'follicular thyroid adenoma'
'thyroid hyalinizing trabecular adenoma' SubClassOf 'thyroid tumor'
'thyroid hyalinizing trabecular adenoma' SubClassOf 'epithelial neoplasm'
'thyroid hyalinizing trabecular adenoma' SubClassOf 'disease arises from structure' some http://purl.obolibrary.org/obo/CL_0002258
http://purl.obolibrary.org/obo/MONDO_0003809
malignant mediastinum hemangiopericytoma
'malignant mediastinum hemangiopericytoma' SubClassOf 'hemangiopericytoma'
'malignant mediastinum hemangiopericytoma' SubClassOf 'mediastinum sarcoma'
'malignant mediastinum hemangiopericytoma' SubClassOf 'mediastinal cancer'
'malignant mediastinum hemangiopericytoma' SubClassOf 'hemangiopericytoma, malignant'
http://purl.obolibrary.org/obo/MONDO_0003825
kidney oncocytoma
'kidney oncocytoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0003842
childhood cerebellar astrocytic neoplasm
'childhood cerebellar astrocytic neoplasm' SubClassOf 'childhood brainstem astrocytoma'
'childhood cerebellar astrocytic neoplasm' SubClassOf 'childhood astrocytic tumor'
http://purl.obolibrary.org/obo/MONDO_0003869
childhood brain stem glioma
'childhood brain stem glioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0013209
non-alcoholic fatty liver disease
'non-alcoholic fatty liver disease' SubClassOf 'fatty liver disease'
'non-alcoholic fatty liver disease' SubClassOf 'fatty liver disease'
http://purl.obolibrary.org/obo/DOID_0080208 EquivalentTo 'non-alcoholic fatty liver disease'
http://purl.obolibrary.org/obo/MONDO_0013225
congenital generalized lipodystrophy type 4
'congenital generalized lipodystrophy type 4' SubClassOf 'genetic lipodystrophy'
http://linkedlifedata.com/resource/umls/id/C1266094
http://linkedlifedata.com/resource/umls/id/C1266094 EquivalentTo 'predominantly cortical thymoma'
http://linkedlifedata.com/resource/umls/id/C1266094 EquivalentTo 'thymoma type B1'
http://purl.obolibrary.org/obo/MONDO_0008414
SCZD1
'SCZD1' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070077 EquivalentTo 'SCZD1'
'SCZD1' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0008482
sprengel deformity (disease)
'sprengel deformity (disease)' SubClassOf 'rare genetic respiratory disease'
http://purl.obolibrary.org/obo/MONDO_0008306
ABri amyloidosis
'ABri amyloidosis' SubClassOf 'cerebral amyloid angiopathy'
'ABri amyloidosis' SubClassOf 'cerebral amyloid angiopathy'
http://purl.obolibrary.org/obo/DOID_0070029 EquivalentTo 'ABri amyloidosis'
http://purl.obolibrary.org/obo/MONDO_0008383
rheumatoid arthritis
'rheumatoid arthritis' EquivalentTo 'arthritis' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'rheumatoid arthritis' EquivalentTo 'arthritis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0008259
familial spontaneous pneumothorax
http://purl.obolibrary.org/obo/DOID_0080218 EquivalentTo 'familial spontaneous pneumothorax'
'familial spontaneous pneumothorax' SubClassOf 'pneumothorax (disease)'
http://purl.obolibrary.org/obo/MONDO_0008292
punctate palmoplantar keratoderma type 2
http://purl.obolibrary.org/obo/DOID_0080213 EquivalentTo 'punctate palmoplantar keratoderma type 2'
http://purl.obolibrary.org/obo/MONDO_0023646
lipodermatosclerosis
'lipodermatosclerosis' SubClassOf 'chronic acquired demyelinating polyneuropathy'
http://purl.obolibrary.org/obo/MONDO_0008086
neuropathy, hereditary sensory and autonomic, type 1A
http://purl.obolibrary.org/obo/DOID_0070152 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 1A'
http://purl.obolibrary.org/obo/MONDO_0008093
nevus, epidermal
http://purl.obolibrary.org/obo/DOID_0111162 EquivalentTo 'nevus, epidermal'
http://purl.obolibrary.org/obo/MONDO_0004107
splenic manifestation of leukemia
'splenic manifestation of leukemia' SubClassOf 'rare digestive tumor'
'splenic manifestation of leukemia' SubClassOf 'rare gastroenterologic disease'
http://purl.obolibrary.org/obo/MONDO_0004105
childhood epithelioid sarcoma
'childhood epithelioid sarcoma' SubClassOf 'childhood malignant neoplasm'
'childhood epithelioid sarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004104
splenic manifestation of hairy cell leukemia
'splenic manifestation of hairy cell leukemia' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0004137
hereditary conventional renal cell carcinoma
http://purl.obolibrary.org/obo/DOID_7192 EquivalentTo 'hereditary conventional renal cell carcinoma'
'hereditary conventional renal cell carcinoma' SubClassOf 'hereditary renal cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0004153
childhood central nervous system embryonal carcinoma
'childhood central nervous system embryonal carcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004193
pediatric ovarian dysgerminoma
'pediatric ovarian dysgerminoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004024
spinal cord neuroblastoma
'spinal cord neuroblastoma' SubClassOf 'spinal cord primitive neuroectodermal tumor'
'spinal cord neuroblastoma' SubClassOf 'spinal cord cancer'
http://purl.obolibrary.org/obo/MONDO_0004036
predominantly cortical thymoma
'predominantly cortical thymoma' SubClassOf 'thymoma type B'
http://linkedlifedata.com/resource/umls/id/C1266094 EquivalentTo 'predominantly cortical thymoma'
http://purl.obolibrary.org/obo/DOID_6917 EquivalentTo 'predominantly cortical thymoma'
http://purl.obolibrary.org/obo/MONDO_0004048
immature gastric teratoma
'immature gastric teratoma' SubClassOf 'extragonadal non-dysgerminomatous germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0004046
childhood brain meningioma
'childhood brain meningioma' SubClassOf 'childhood malignant neoplasm'
'childhood brain meningioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004045
pediatric intraocular retinoblastoma
'pediatric intraocular retinoblastoma' SubClassOf 'childhood malignant neoplasm'
'pediatric intraocular retinoblastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004071
childhood cerebral astrocytoma
'childhood cerebral astrocytoma' SubClassOf 'childhood malignant neoplasm'
'childhood cerebral astrocytoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004077
lumbosacral lipoma
'lumbosacral lipoma' SubClassOf 'lipoma'
'lumbosacral lipoma' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0006075
'lumbosacral lipoma' SubClassOf 'vertebral column disease'
'lumbosacral lipoma' SubClassOf 'disorder of anatomical region'
'lumbosacral lipoma' EquivalentTo 'lipoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0006075)
http://purl.obolibrary.org/obo/MONDO_0004082
childhood immature teratoma of ovary
'childhood immature teratoma of ovary' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0018544
X-linked adrenoleukodystrophy
'X-linked adrenoleukodystrophy' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0018580
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
'PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome' SubClassOf 'rare genetic syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0018598
neonatal adrenoleukodystrophy
'neonatal adrenoleukodystrophy' SubClassOf 'rare genetic epilepsy'
http://linkedlifedata.com/resource/umls/id/C1516437
http://linkedlifedata.com/resource/umls/id/C1516437 EquivalentTo 'cervical wilms' tumor'
http://linkedlifedata.com/resource/umls/id/C1516437 EquivalentTo 'cervical wilms tumor'
http://purl.obolibrary.org/obo/MONDO_0018465
insulin autoimmune syndrome
http://purl.obolibrary.org/obo/DOID_0040100 EquivalentTo 'insulin autoimmune syndrome'
'insulin autoimmune syndrome' SubClassOf 'autoimmune disease of endocrine system'
'insulin autoimmune syndrome' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/MONDO_0018492
hereditary clear cell renal cell carcinoma
'hereditary clear cell renal cell carcinoma' SubClassOf 'hereditary renal cell carcinoma'
http://purl.obolibrary.org/obo/DOID_7192 EquivalentTo 'hereditary clear cell renal cell carcinoma'
'hereditary clear cell renal cell carcinoma' SubClassOf 'hereditary renal cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0018489
autoimmune encephalopathy with parasomnia and obstructive sleep apnea
'autoimmune encephalopathy with parasomnia and obstructive sleep apnea' EquivalentTo 'brain disease' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002870) and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960) and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0025234)
'autoimmune encephalopathy with parasomnia and obstructive sleep apnea' SubClassOf 'disease arises from feature' some http://purl.obolibrary.org/obo/HP_0025234
'autoimmune encephalopathy with parasomnia and obstructive sleep apnea' SubClassOf 'autoimmune disease of central nervous system'
'autoimmune encephalopathy with parasomnia and obstructive sleep apnea' SubClassOf 'disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002870
'autoimmune encephalopathy with parasomnia and obstructive sleep apnea' SubClassOf 'brain disease'
'autoimmune encephalopathy with parasomnia and obstructive sleep apnea' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/MONDO_0018304
Schnitzler syndrome
'Schnitzler syndrome' SubClassOf 'rare urticaria'
'Schnitzler syndrome' SubClassOf 'autoimmune disease of musculoskeletal system'
'Schnitzler syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0025513
http://purl.obolibrary.org/obo/MONDO_0018334
chronic hiccup
'chronic hiccup' SubClassOf 'disease has major feature' some http://purl.obolibrary.org/obo/HP_0100247
'chronic hiccup' EquivalentTo 'autonomic nervous system disease' and ('disease has major feature' some http://purl.obolibrary.org/obo/HP_0100247)
http://purl.obolibrary.org/obo/MONDO_0018369
immature ovarian teratoma
'immature ovarian teratoma' SubClassOf 'malignant germ cell tumor of ovary'
'immature ovarian teratoma' SubClassOf 'malignant non-dysgerminomatous germ cell tumor of ovary'
http://purl.obolibrary.org/obo/DOID_11217
http://purl.obolibrary.org/obo/DOID_11217 EquivalentTo 'chronic tympanitis'
http://purl.obolibrary.org/obo/DOID_11217 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0001227ub
http://purl.obolibrary.org/obo/MONDO_0008869
Seckel syndrome 1
'Seckel syndrome 1' SubClassOf 'Seckel syndrome'
'Seckel syndrome 1' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070007 EquivalentTo 'Seckel syndrome 1'
http://purl.obolibrary.org/obo/MONDO_0018213
hereditary sensory and autonomic neuropathy type 1
http://purl.obolibrary.org/obo/DOID_0070162 EquivalentTo 'hereditary sensory and autonomic neuropathy type 1'
http://purl.obolibrary.org/obo/MONDO_0018242
autoimmune hypoparathyroidism (disease)
'autoimmune hypoparathyroidism (disease)' SubClassOf 'autoimmune disease of endocrine system'
'autoimmune hypoparathyroidism (disease)' EquivalentTo 'hypoparathyroidism' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune hypoparathyroidism (disease)' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/MONDO_0008747
oculocutaneous albinism type 3
'oculocutaneous albinism type 3' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/DOID_0070097 EquivalentTo 'oculocutaneous albinism type 3'
'oculocutaneous albinism type 3' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/MONDO_0008746
oculocutaneous albinism type 2
'oculocutaneous albinism type 2' SubClassOf 'oculocutaneous albinism'
'oculocutaneous albinism type 2' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/DOID_0070096 EquivalentTo 'oculocutaneous albinism type 2'
http://purl.obolibrary.org/obo/MONDO_0008745
oculocutaneous albinism type 1A
http://purl.obolibrary.org/obo/DOID_0070094 EquivalentTo 'oculocutaneous albinism type 1A'
http://purl.obolibrary.org/obo/MONDO_0018163
autosomal recessive cutis laxa type 2A
http://purl.obolibrary.org/obo/DOID_0070134 EquivalentTo 'autosomal recessive cutis laxa type 2A'
http://purl.obolibrary.org/obo/MONDO_0008608
down syndrome
'down syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0008657
vibratory angioedema
'vibratory angioedema' SubClassOf 'rare genetic immune disease'
http://purl.obolibrary.org/obo/MONDO_0008684
Wolf-Hirschhorn syndrome
'Wolf-Hirschhorn syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'Wolf-Hirschhorn syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0018092
Vogt-Koyanagi-Harada disease
'Vogt-Koyanagi-Harada disease' SubClassOf 'autoimmune disease of the nervous system'
'Vogt-Koyanagi-Harada disease' SubClassOf 'genetic otorhinolaryngologic disease'
'Vogt-Koyanagi-Harada disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0031012
http://purl.obolibrary.org/obo/MONDO_0018097
West syndrome
'West syndrome' SubClassOf 'infantile epilepsy syndrome'
'West syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100022
http://purl.obolibrary.org/obo/MONDO_0014336
intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
http://purl.obolibrary.org/obo/DOID_0070053 EquivalentTo 'intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency'
http://purl.obolibrary.org/obo/MONDO_0014357
mental retardation, autosomal dominant 24
'mental retardation, autosomal dominant 24' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070054 EquivalentTo 'mental retardation, autosomal dominant 24'
'mental retardation, autosomal dominant 24' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0014358
AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome
http://purl.obolibrary.org/obo/DOID_0070055 EquivalentTo 'AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome'
http://purl.obolibrary.org/obo/MONDO_0014350
Seckel syndrome 8
'Seckel syndrome 8' SubClassOf 'Seckel syndrome'
'Seckel syndrome 8' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070009 EquivalentTo 'Seckel syndrome 8'
http://purl.obolibrary.org/obo/MONDO_0014361
autism spectrum disorder due to AUTS2 deficiency
http://purl.obolibrary.org/obo/DOID_0070056 EquivalentTo 'autism spectrum disorder due to AUTS2 deficiency'
http://purl.obolibrary.org/obo/MONDO_0014379
ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder
http://purl.obolibrary.org/obo/DOID_0070058 EquivalentTo 'ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder'
http://purl.obolibrary.org/obo/MONDO_0014376
mental retardation, autosomal dominant 27
http://purl.obolibrary.org/obo/DOID_0070057 EquivalentTo 'mental retardation, autosomal dominant 27'
http://purl.obolibrary.org/obo/MONDO_0014414
STAT3-related early-onset multisystem autoimmune disease
'STAT3-related early-onset multisystem autoimmune disease' SubClassOf 'lymphoproliferative syndrome'
'STAT3-related early-onset multisystem autoimmune disease' SubClassOf 'rare genetic inherited tumor'
'STAT3-related early-onset multisystem autoimmune disease' SubClassOf 'autoimmune lymphoproliferative syndrome'
http://purl.obolibrary.org/obo/MONDO_0014213
intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome
http://purl.obolibrary.org/obo/DOID_0070051 EquivalentTo 'intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome'
http://purl.obolibrary.org/obo/MONDO_0014212
sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
http://purl.obolibrary.org/obo/DOID_0111166 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type C'
http://purl.obolibrary.org/obo/MONDO_0014244
hereditary sensory and autonomic neuropathy type 7
http://purl.obolibrary.org/obo/DOID_0070149 EquivalentTo 'hereditary sensory and autonomic neuropathy type 7'
http://purl.obolibrary.org/obo/MONDO_0014286
neuropathy, hereditary sensory, type 1F
http://purl.obolibrary.org/obo/DOID_0070154 EquivalentTo 'neuropathy, hereditary sensory, type 1F'
http://purl.obolibrary.org/obo/MONDO_0004923
chronic inflammation of lacrimal passage
'chronic inflammation of lacrimal passage' EquivalentTo 'disease' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863) and ('disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0001850)
'chronic inflammation of lacrimal passage' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
http://purl.obolibrary.org/obo/MONDO_0004925
chronic dacryocystitis
'chronic dacryocystitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
http://purl.obolibrary.org/obo/MONDO_0004924
chronic canaliculitis
'chronic canaliculitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
http://purl.obolibrary.org/obo/MONDO_0004977
angioimmunoblastic T-cell lymphoma
'angioimmunoblastic T-cell lymphoma' SubClassOf 'mature T-cell and NK-cell non-Hodgkin lymphoma'
http://purl.obolibrary.org/obo/DOID_0111147 EquivalentTo 'angioimmunoblastic T-cell lymphoma'
'angioimmunoblastic T-cell lymphoma' SubClassOf 'peripheral T-cell lymphoma'
http://purl.obolibrary.org/obo/MONDO_0004971
adenoid cystic carcinoma
'adenoid cystic carcinoma' SubClassOf 'carcinoma'
'adenoid cystic carcinoma' SubClassOf 'adenocarcinoma'
http://purl.obolibrary.org/obo/DOID_0080202 EquivalentTo 'adenoid cystic carcinoma'
http://purl.obolibrary.org/obo/MONDO_0004795
otitis externa
'otitis externa' SubClassOf 'post-infectious disorder'
http://purl.obolibrary.org/obo/MONDO_0014127
oculocutaneous albinism type 5
'oculocutaneous albinism type 5' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/DOID_0070099 EquivalentTo 'oculocutaneous albinism type 5'
'oculocutaneous albinism type 5' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/MONDO_0014005
immunoglobulin-mediated membranoproliferative glomerulonephritis
'immunoglobulin-mediated membranoproliferative glomerulonephritis' SubClassOf 'inborn errors of metabolism'
http://purl.obolibrary.org/obo/MONDO_0014006
intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome
http://purl.obolibrary.org/obo/DOID_0070047 EquivalentTo 'intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome'
http://purl.obolibrary.org/obo/MONDO_0014035
severe intellectual disability-progressive spastic diplegia syndrome
http://purl.obolibrary.org/obo/DOID_0070049 EquivalentTo 'severe intellectual disability-progressive spastic diplegia syndrome'
http://purl.obolibrary.org/obo/MONDO_0014034
severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
http://purl.obolibrary.org/obo/DOID_0070048 EquivalentTo 'severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome'
http://purl.obolibrary.org/obo/MONDO_0014070
oculocutaneous albinism type 7
'oculocutaneous albinism type 7' SubClassOf 'oculocutaneous albinism'
'oculocutaneous albinism type 7' SubClassOf 'oculocutaneous albinism'
http://purl.obolibrary.org/obo/DOID_0070100 EquivalentTo 'oculocutaneous albinism type 7'
http://purl.obolibrary.org/obo/MONDO_0014076
dyskeratosis congenita, autosomal recessive 5
'dyskeratosis congenita, autosomal recessive 5' SubClassOf 'Hoyeraal-Hreidarsson syndrome'
http://purl.obolibrary.org/obo/DOID_0070022 EquivalentTo 'dyskeratosis congenita, autosomal recessive 5'
'dyskeratosis congenita, autosomal recessive 5' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070020 EquivalentTo 'dyskeratosis congenita, autosomal recessive 5'
http://purl.obolibrary.org/obo/MONDO_0014092
schizophrenia 18
'schizophrenia 18' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070093 EquivalentTo 'schizophrenia 18'
'schizophrenia 18' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0004757
chronic ethmoidal sinusitis
'chronic ethmoidal sinusitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic ethmoidal sinusitis' SubClassOf 'chronic rhinosinusitis'
http://purl.obolibrary.org/obo/MONDO_0004525
scabies
'scabies' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_52283
'scabies' EquivalentTo 'disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_52283)
http://purl.obolibrary.org/obo/MONDO_0004535
childhood choriocarcinoma of the ovary
'childhood choriocarcinoma of the ovary' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004423
central nervous system extraskeletal osteosarcoma
'central nervous system extraskeletal osteosarcoma' SubClassOf 'central nervous system mesenchymal non-meningothelial tumor'
'central nervous system extraskeletal osteosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037740
http://purl.obolibrary.org/obo/MONDO_0004436
ovarian myxoid liposarcoma
'ovarian myxoid liposarcoma' SubClassOf 'ovary leiomyosarcoma'
http://purl.obolibrary.org/obo/MONDO_0004441
childhood ovarian embryonal carcinoma
'childhood ovarian embryonal carcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004491
uterine corpus choriocarcinoma
'uterine corpus choriocarcinoma' SubClassOf 'uterine corpus cancer'
'uterine corpus choriocarcinoma' SubClassOf 'mixed germ cell cancer'
'uterine corpus choriocarcinoma' SubClassOf 'rare uterine cancer'
'uterine corpus choriocarcinoma' SubClassOf 'malignant germ cell tumor of corpus uteri'
http://purl.obolibrary.org/obo/MONDO_0004490
gestational uterine corpus choriocarcinoma
'gestational uterine corpus choriocarcinoma' SubClassOf 'malignant germ cell tumor of corpus uteri'
http://purl.obolibrary.org/obo/MONDO_0018943
myofibrillar myopathy (disease)
http://purl.obolibrary.org/obo/DOID_0080307 EquivalentTo 'myofibrillar myopathy (disease)'
http://purl.obolibrary.org/obo/MONDO_0004308
meninges sarcoma
'meninges sarcoma' SubClassOf 'meningioma (disease)'
http://purl.obolibrary.org/obo/MONDO_0004325
testicular thecoma
'testicular thecoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037252
'testicular thecoma' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037252 and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000473)
http://purl.obolibrary.org/obo/MONDO_0004345
childhood malignant schwannoma
'childhood malignant schwannoma' SubClassOf 'childhood malignant neoplasm'
'childhood malignant schwannoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004355
childhood leukemia
'childhood leukemia' SubClassOf 'childhood malignant neoplasm'
'childhood leukemia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004350
pediatric extraocular retinoblastoma
'pediatric extraocular retinoblastoma' SubClassOf 'childhood malignant neoplasm'
'pediatric extraocular retinoblastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004394
maxillary sinus squamous cell carcinoma
'maxillary sinus squamous cell carcinoma' SubClassOf 'rare bone disease'
'maxillary sinus squamous cell carcinoma' SubClassOf 'rare respiratory disease'
'maxillary sinus squamous cell carcinoma' SubClassOf 'rare nervous system tumor'
'maxillary sinus squamous cell carcinoma' SubClassOf 'bone squamous cell carcinoma'
http://linkedlifedata.com/resource/umls/id/C0021070
http://linkedlifedata.com/resource/umls/id/C0021070 EquivalentTo 'hypersensitivity reaction type IV disease'
http://purl.obolibrary.org/obo/MONDO_0004221
uterine corpus perivascular epithelioid cell tumor
'uterine corpus perivascular epithelioid cell tumor' SubClassOf 'uterine corpus cancer'
'uterine corpus perivascular epithelioid cell tumor' SubClassOf 'corpus uteri neoplasm'
http://purl.obolibrary.org/obo/MONDO_0004239
cervical keratinizing squamous cell carcinoma
'cervical keratinizing squamous cell carcinoma' EquivalentTo 'keratinizing squamous cell carcinoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000002)
http://purl.obolibrary.org/obo/MONDO_0004233
childhood pleomorphic rhabdomyosarcoma
'childhood pleomorphic rhabdomyosarcoma' SubClassOf 'childhood malignant neoplasm'
'childhood pleomorphic rhabdomyosarcoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004248
pediatric infratentorial ependymoma
'pediatric infratentorial ependymoma' SubClassOf 'childhood malignant neoplasm'
'pediatric infratentorial ependymoma' SubClassOf 'infratentorial cancer'
http://purl.obolibrary.org/obo/MONDO_0004240
posterior urethra cancer
'posterior urethra cancer' SubClassOf 'female urethral cancer'
'posterior urethra cancer' SubClassOf 'urethra cancer'
http://purl.obolibrary.org/obo/MONDO_0004257
childhood central nervous system mixed germ cell tumor
'childhood central nervous system mixed germ cell tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0004252
small intestinal L-cell glucagon-like peptide producing tumor
'small intestinal L-cell glucagon-like peptide producing tumor' SubClassOf 'malignant endocrine neoplasm'
'small intestinal L-cell glucagon-like peptide producing tumor' SubClassOf 'small intestine cancer'
http://purl.obolibrary.org/obo/MONDO_0018893
Cobb syndrome
'Cobb syndrome' SubClassOf 'nervous system benign neoplasm'
'Cobb syndrome' SubClassOf 'genetic nervous system disorder'
'Cobb syndrome' SubClassOf 'intracranial hemangioma'
'Cobb syndrome' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0018892
Wyburn-Mason syndrome
'Wyburn-Mason syndrome' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0004263
pediatric infratentorial ependymoblastoma
'pediatric infratentorial ependymoblastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
'pediatric infratentorial ependymoblastoma' SubClassOf 'childhood central nervous system primitive neuroectodermal neoplasm'
'pediatric infratentorial ependymoblastoma' SubClassOf 'infratentorial cancer'
http://purl.obolibrary.org/obo/MONDO_0018907
craniopharyngioma
'craniopharyngioma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0018902
hepatocellular adenoma
'hepatocellular adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0000605
hypersensitivity reaction disease
'hypersensitivity reaction disease' SubClassOf 'immune system disease'
'hypersensitivity reaction disease' SubClassOf 'immune system disease'
'hypersensitivity reaction disease' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3114
http://purl.obolibrary.org/obo/MONDO_0024676
childhood kidney wilms tumor
'childhood kidney wilms tumor' SubClassOf 'childhood malignant neoplasm'
'childhood kidney wilms tumor' SubClassOf 'childhood kidney neoplasm'
'childhood kidney wilms tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036511
'childhood kidney wilms tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0024666
benign epithelial skin neoplasm
'benign epithelial skin neoplasm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0009054
autosomal recessive cutis laxa type 2, classic type
http://purl.obolibrary.org/obo/DOID_0070141 EquivalentTo 'autosomal recessive cutis laxa type 2, classic type'
http://purl.obolibrary.org/obo/DOID_0070136 EquivalentTo 'autosomal recessive cutis laxa type 2, classic type'
http://purl.obolibrary.org/obo/MONDO_0009053
ALDH18A1-related de Barsy syndrome
http://purl.obolibrary.org/obo/DOID_0070132 EquivalentTo 'ALDH18A1-related de Barsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0009052
cutis laxa, autosomal recessive, type 1A
http://purl.obolibrary.org/obo/DOID_0070135 EquivalentTo 'cutis laxa, autosomal recessive, type 1A'
http://purl.obolibrary.org/obo/MONDO_0009050
ACTH-secreting pituitary adenoma
'ACTH-secreting pituitary adenoma' SubClassOf 'benign male reproductive system neoplasm'
'ACTH-secreting pituitary adenoma' SubClassOf 'cardiovascular organ benign neoplasm'
http://purl.obolibrary.org/obo/MONDO_0000515
bone chondrosarcoma
'bone chondrosarcoma' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0000514
bone squamous cell carcinoma
'bone squamous cell carcinoma' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0000524
mixed extragonadal germ cell cancer
'mixed extragonadal germ cell cancer' SubClassOf 'mixed germ cell cancer'
'mixed extragonadal germ cell cancer' EquivalentTo 'mixed germ cell tumor' and 'extragonadal germ cell tumor'
'mixed extragonadal germ cell cancer' SubClassOf 'extragonadal germ cell cancer'
'mixed extragonadal germ cell cancer' SubClassOf 'mixed germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0000538
spindle epithelial tumor with thymus-like differentiation tumor
http://purl.obolibrary.org/obo/DOID_0050923 EquivalentTo 'spindle epithelial tumor with thymus-like differentiation tumor'
'spindle epithelial tumor with thymus-like differentiation tumor' SubClassOf 'thyroid gland carcinoma'
http://purl.obolibrary.org/obo/MONDO_0000587
autoimmune disease of ear, nose and throat
'autoimmune disease of ear, nose and throat' EquivalentTo 'otorhinolaryngologic disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune disease of ear, nose and throat' EquivalentTo 'otorhinolaryngologic disease' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0024377
circadian rhythm sleep disorder, delayed sleep phase type
http://purl.obolibrary.org/obo/DOID_0111141 EquivalentTo 'circadian rhythm sleep disorder, delayed sleep phase type'
http://purl.obolibrary.org/obo/MONDO_0000437
cerebellar ataxia
'cerebellar ataxia' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_164400
http://purl.obolibrary.org/obo/MONDO_0000456
cerebral creatine deficiency syndrome
'cerebral creatine deficiency syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/MONDO_0024264
hypothyroidism, congenital, nongoitrous, 2
http://purl.obolibrary.org/obo/DOID_0070124 EquivalentTo 'hypothyroidism, congenital, nongoitrous, 2'
http://purl.obolibrary.org/obo/MONDO_0014922
myofibrillar myopathy 7
'myofibrillar myopathy 7' SubClassOf 'myofibrillar myopathy (disease)'
'myofibrillar myopathy 7' SubClassOf 'myofibrillar myopathy (disease)'
http://purl.obolibrary.org/obo/DOID_0080098 EquivalentTo 'myofibrillar myopathy 7'
http://purl.obolibrary.org/obo/MONDO_0024311
cancer affecting bone of limb skeleton
'cancer affecting bone of limb skeleton' SubClassOf 'bone disease'
http://purl.obolibrary.org/obo/MONDO_0014993
myopathy, myofibrillar, 8; MFM8
http://purl.obolibrary.org/obo/DOID_0080308 EquivalentTo 'myopathy, myofibrillar, 8; MFM8'
http://purl.obolibrary.org/obo/MONDO_0024309
neuropathy, hereditary sensory and autonomic, type 2A
http://purl.obolibrary.org/obo/DOID_0070155 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 2A'
http://purl.obolibrary.org/obo/MONDO_0014991
Seckel syndrome 10; SCKL10
'Seckel syndrome 10; SCKL10' SubClassOf 'Seckel syndrome'
'Seckel syndrome 10; SCKL10' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070008 EquivalentTo 'Seckel syndrome 10; SCKL10'
http://purl.obolibrary.org/obo/MONDO_0024337
urothelial neoplasm
'urothelial neoplasm' SubClassOf 'epithelial neoplasm'
'urothelial neoplasm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037254
http://purl.obolibrary.org/obo/MONDO_0024330
infectious otitis media
'infectious otitis media' SubClassOf 'infectious disease of the nervous system'
'infectious otitis media' SubClassOf 'rare otorhinolaryngologic disease'
http://purl.obolibrary.org/obo/MONDO_0024323
glomangiomyoma
'glomangiomyoma' SubClassOf 'rare circulatory system disease'
'glomangiomyoma' SubClassOf 'benign perivascular tumor'
http://purl.obolibrary.org/obo/MONDO_0024325
cutaneous glomangiomyoma
'cutaneous glomangiomyoma' SubClassOf 'benign neoplasm of skin'
http://purl.obolibrary.org/obo/MONDO_0024358
complex sleep apnea
http://purl.obolibrary.org/obo/DOID_0080302 EquivalentTo 'complex sleep apnea'
http://purl.obolibrary.org/obo/MONDO_0000380
paranasal sinus carcinoma
'paranasal sinus carcinoma' SubClassOf 'rare nervous system tumor'
'paranasal sinus carcinoma' SubClassOf 'rare respiratory disease'
http://purl.obolibrary.org/obo/MONDO_0000188
GLUT1 deficiency syndrome
'GLUT1 deficiency syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
'GLUT1 deficiency syndrome' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0014837
hereditary thrombocytopenia with early-onset myelofibrosis
'hereditary thrombocytopenia with early-onset myelofibrosis' SubClassOf 'rare genetic inherited tumor'
'hereditary thrombocytopenia with early-onset myelofibrosis' SubClassOf 'rare genetic bone disease'
'hereditary thrombocytopenia with early-onset myelofibrosis' SubClassOf 'inherited syndrome with bone tumors as a major feature'
http://purl.obolibrary.org/obo/MONDO_0014842
mental retardation, autosomal dominant 41; MRD41
'mental retardation, autosomal dominant 41; MRD41' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070071 EquivalentTo 'mental retardation, autosomal dominant 41; MRD41'
'mental retardation, autosomal dominant 41; MRD41' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0014858
mental retardation, autosomal dominant 43; MRD43
'mental retardation, autosomal dominant 43; MRD43' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070073 EquivalentTo 'mental retardation, autosomal dominant 43; MRD43'
'mental retardation, autosomal dominant 43; MRD43' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0014855
mental retardation, autosomal dominant 42; MRD42
'mental retardation, autosomal dominant 42; MRD42' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070072 EquivalentTo 'mental retardation, autosomal dominant 42; MRD42'
'mental retardation, autosomal dominant 42; MRD42' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0014892
micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome
http://purl.obolibrary.org/obo/DOID_0070074 EquivalentTo 'micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome'
http://purl.obolibrary.org/obo/MONDO_0024235
Brenner tumor
'Brenner tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037254
http://purl.obolibrary.org/obo/MONDO_0000262
otomycosis
'otomycosis' SubClassOf 'infectious disease of the nervous system'
'otomycosis' SubClassOf 'rare otorhinolaryngologic disease'
http://purl.obolibrary.org/obo/MONDO_0014699
mental retardation, autosomal dominant 40
'mental retardation, autosomal dominant 40' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 40' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070070 EquivalentTo 'mental retardation, autosomal dominant 40'
http://purl.obolibrary.org/obo/MONDO_0014690
dyskeratosis congenita, autosomal dominant 6
'dyskeratosis congenita, autosomal dominant 6' SubClassOf 'Hoyeraal-Hreidarsson syndrome'
'dyskeratosis congenita, autosomal dominant 6' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070023 EquivalentTo 'dyskeratosis congenita, autosomal dominant 6'
http://purl.obolibrary.org/obo/MONDO_0014706
cutis laxa, autosomal dominant 3
http://purl.obolibrary.org/obo/DOID_0070131 EquivalentTo 'cutis laxa, autosomal dominant 3'
http://purl.obolibrary.org/obo/MONDO_0014708
ring chromosome 14
'ring chromosome 14' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'ring chromosome 14' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0014707
14q32 duplication syndrome
'14q32 duplication syndrome' SubClassOf 'rare genetic inherited tumor'
'14q32 duplication syndrome' SubClassOf 'rare genetic bone disease'
'14q32 duplication syndrome' SubClassOf 'inherited syndrome with bone tumors as a major feature'
http://purl.obolibrary.org/obo/MONDO_0014744
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
http://purl.obolibrary.org/obo/DOID_0111155 EquivalentTo 'acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome'
http://purl.obolibrary.org/obo/MONDO_0014767
Seckel syndrome 9; SCKL9
'Seckel syndrome 9; SCKL9' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070005 EquivalentTo 'Seckel syndrome 9; SCKL9'
'Seckel syndrome 9; SCKL9' SubClassOf 'Seckel syndrome'
http://purl.obolibrary.org/obo/MONDO_0014580
mental retardation, autosomal dominant 33
'mental retardation, autosomal dominant 33' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 33' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070063 EquivalentTo 'mental retardation, autosomal dominant 33'
http://purl.obolibrary.org/obo/MONDO_0014599
mental retardation, autosomal dominant 34
'mental retardation, autosomal dominant 34' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070064 EquivalentTo 'mental retardation, autosomal dominant 34'
'mental retardation, autosomal dominant 34' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0014606
intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
http://purl.obolibrary.org/obo/DOID_0070067 EquivalentTo 'intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome'
http://purl.obolibrary.org/obo/MONDO_0014605
microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome
http://purl.obolibrary.org/obo/DOID_0070066 EquivalentTo 'microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome'
http://purl.obolibrary.org/obo/MONDO_0014602
intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome
http://purl.obolibrary.org/obo/DOID_0070065 EquivalentTo 'intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome'
http://purl.obolibrary.org/obo/MONDO_0014600
dyskeratosis congenita, autosomal recessive 6
'dyskeratosis congenita, autosomal recessive 6' SubClassOf 'Hoyeraal-Hreidarsson syndrome'
'dyskeratosis congenita, autosomal recessive 6' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070024 EquivalentTo 'dyskeratosis congenita, autosomal recessive 6'
http://purl.obolibrary.org/obo/MONDO_0014617
mental retardation, autosomal dominant 38
'mental retardation, autosomal dominant 38' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 38' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070068 EquivalentTo 'mental retardation, autosomal dominant 38'
http://purl.obolibrary.org/obo/MONDO_0014658
severe achondroplasia-developmental delay-acanthosis nigricans syndrome
http://purl.obolibrary.org/obo/DOID_0111158 EquivalentTo 'severe achondroplasia-developmental delay-acanthosis nigricans syndrome'
'severe achondroplasia-developmental delay-acanthosis nigricans syndrome' SubClassOf 'autosomal dominant disease'
http://purl.obolibrary.org/obo/MONDO_0014662
congenital insensitivity to pain-hypohidrosis syndrome
http://purl.obolibrary.org/obo/DOID_0070153 EquivalentTo 'congenital insensitivity to pain-hypohidrosis syndrome'
http://purl.obolibrary.org/obo/MONDO_0014678
mental retardation, autosomal dominant 39
'mental retardation, autosomal dominant 39' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'mental retardation, autosomal dominant 39' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070069 EquivalentTo 'mental retardation, autosomal dominant 39'
http://purl.obolibrary.org/obo/MONDO_0014471
isolated ATP synthase deficiency
http://purl.obolibrary.org/obo/DOID_0111143 EquivalentTo 'isolated ATP synthase deficiency'
'isolated ATP synthase deficiency' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/GO_0005753
'isolated ATP synthase deficiency' EquivalentTo 'disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/GO_0005753)
http://purl.obolibrary.org/obo/MONDO_0014487
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
http://purl.obolibrary.org/obo/DOID_0080209 EquivalentTo 'congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome'
http://purl.obolibrary.org/obo/MONDO_0014486
mental retardation, autosomal dominant 30
http://purl.obolibrary.org/obo/DOID_0070060 EquivalentTo 'mental retardation, autosomal dominant 30'
http://purl.obolibrary.org/obo/MONDO_0014482
mental retardation, autosomal dominant 29
http://purl.obolibrary.org/obo/DOID_0070059 EquivalentTo 'mental retardation, autosomal dominant 29'
http://purl.obolibrary.org/obo/MONDO_0014493
autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
'autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency' SubClassOf 'hypersensitivity reaction type II disease'
http://purl.obolibrary.org/obo/MONDO_0014510
severe intellectual disability-epilepsy-cataract syndrome due to fatty acyl-CoA reductase 1 deficiency
'severe intellectual disability-epilepsy-cataract syndrome due to fatty acyl-CoA reductase 1 deficiency' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0014512
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation
http://purl.obolibrary.org/obo/DOID_0070061 EquivalentTo 'PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation'
http://purl.obolibrary.org/obo/MONDO_0014558
autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
http://purl.obolibrary.org/obo/DOID_0070062 EquivalentTo 'autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome'
http://purl.obolibrary.org/obo/MONDO_0009807
osteosarcoma (disease)
'osteosarcoma (disease)' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0010826
childhood absence epilepsy
'childhood absence epilepsy' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0009889
autosomal recessive polycystic kidney disease
'autosomal recessive polycystic kidney disease' EquivalentTo http://purl.obolibrary.org/obo/OMIM_263200
http://purl.obolibrary.org/obo/MONDO_0019208
Bickerstaff brainstem encephalitis
'Bickerstaff brainstem encephalitis' SubClassOf 'autoimmune disease of central nervous system'
http://purl.obolibrary.org/obo/MONDO_0010897
SCZD3
'SCZD3' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070079 EquivalentTo 'SCZD3'
'SCZD3' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0019262
juvenile neuronal ceroid lipofuscinosis
'juvenile neuronal ceroid lipofuscinosis' SubClassOf 'neuronal ceroid lipofuscinosis'
http://purl.obolibrary.org/obo/DOID_0050756 EquivalentTo 'juvenile neuronal ceroid lipofuscinosis'
'juvenile neuronal ceroid lipofuscinosis' SubClassOf 'neuronal ceroid lipofuscinosis'
http://purl.obolibrary.org/obo/MONDO_0019298
rare urticaria
'rare urticaria' SubClassOf 'rare allergic disease'
'rare urticaria' SubClassOf 'allergic urticaria'
'rare urticaria' SubClassOf 'urticaria (disease)'
http://purl.obolibrary.org/obo/MONDO_0009746
hereditary sensory and autonomic neuropathy type 4
http://purl.obolibrary.org/obo/DOID_0070146 EquivalentTo 'hereditary sensory and autonomic neuropathy type 4'
http://purl.obolibrary.org/obo/MONDO_0009757
Niemann-Pick disease, type C1
http://purl.obolibrary.org/obo/DOID_0070113 EquivalentTo 'Niemann-Pick disease, type C1'
http://purl.obolibrary.org/obo/MONDO_0009756
Niemann-Pick disease type A
'Niemann-Pick disease type A' SubClassOf 'Niemann-Pick disease'
'Niemann-Pick disease type A' SubClassOf 'Niemann-Pick disease'
http://purl.obolibrary.org/obo/DOID_0070111 EquivalentTo 'Niemann-Pick disease type A'
http://purl.obolibrary.org/obo/MONDO_0009751
neuropathy, hereditary sensory, atypical
'neuropathy, hereditary sensory, atypical' SubClassOf 'hereditary sensory and autonomic neuropathy'
http://purl.obolibrary.org/obo/DOID_0070160 EquivalentTo 'neuropathy, hereditary sensory, atypical'
'neuropathy, hereditary sensory, atypical' SubClassOf 'hereditary sensory and autonomic neuropathy'
http://purl.obolibrary.org/obo/MONDO_0019101
retinal capillary malformation
'retinal capillary malformation' SubClassOf 'rare genetic epilepsy'
'retinal capillary malformation' SubClassOf 'brain neoplasm'
http://purl.obolibrary.org/obo/MONDO_0020108
autoimmune hemolytic anemia
'autoimmune hemolytic anemia' EquivalentTo 'hemolytic anemia' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune hemolytic anemia' EquivalentTo 'hemolytic anemia' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0020122
idiopathic inflammatory myopathy
'idiopathic inflammatory myopathy' SubClassOf 'autoimmune disease of peripheral nervous system'
'idiopathic inflammatory myopathy' SubClassOf 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/MONDO_0019174
infantile Refsum disease
'infantile Refsum disease' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0019180
hereditary hemorrhagic telangiectasia
'hereditary hemorrhagic telangiectasia' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0019193
acquired generalized lipodystrophy
'acquired generalized lipodystrophy' SubClassOf 'acquired carbohydrate metabolism disease'
http://purl.obolibrary.org/obo/DOID_0080300 EquivalentTo 'acquired generalized lipodystrophy'
'acquired generalized lipodystrophy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0027766
'acquired generalized lipodystrophy' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0027766 and ('has modifier' some 'acquired')
http://purl.obolibrary.org/obo/MONDO_0019196
Foix-Alajouanine syndrome
'Foix-Alajouanine syndrome' SubClassOf 'nervous system benign neoplasm'
'Foix-Alajouanine syndrome' SubClassOf 'intracranial hemangioma'
http://purl.obolibrary.org/obo/MONDO_0019198
sympathetic ophthalmia
'sympathetic ophthalmia' SubClassOf 'autoimmune disease of the nervous system'
'sympathetic ophthalmia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0031012
http://purl.obolibrary.org/obo/MONDO_0019197
folinic acid-responsive seizures
'folinic acid-responsive seizures' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/MONDO_0009627
Galloway-Mowat syndrome
'Galloway-Mowat syndrome' EquivalentTo http://purl.obolibrary.org/obo/OMIM_251300
http://purl.obolibrary.org/obo/MONDO_0009644
sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
http://purl.obolibrary.org/obo/DOID_0111163 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type B'
http://purl.obolibrary.org/obo/MONDO_0009643
sulfite oxidase deficiency due to molybdenum cofactor deficiency type A
http://purl.obolibrary.org/obo/DOID_0111164 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type A'
http://purl.obolibrary.org/obo/MONDO_0009640
mitochondrial complex I deficiency
'mitochondrial complex I deficiency' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/GO_0005747
'mitochondrial complex I deficiency' EquivalentTo 'disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/GO_0005747)
http://purl.obolibrary.org/obo/MONDO_0010648
MAFD2
'MAFD2' SubClassOf 'bipolar disorder'
http://purl.obolibrary.org/obo/DOID_0080221 EquivalentTo 'MAFD2'
'MAFD2' SubClassOf 'bipolar II disorder'
http://purl.obolibrary.org/obo/MONDO_0009666
holocarboxylase synthetase deficiency
'holocarboxylase synthetase deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
'holocarboxylase synthetase deficiency' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0010655
X-linked intellectual disability with marfanoid habitus
'X-linked intellectual disability with marfanoid habitus' SubClassOf 'MED12-related intellectual disability syndrome'
'X-linked intellectual disability with marfanoid habitus' SubClassOf 'MED12-related intellectual disability syndrome'
http://purl.obolibrary.org/obo/MONDO_0009665
biotinidase deficiency
'biotinidase deficiency' SubClassOf 'rare genetic epilepsy'
'biotinidase deficiency' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/DOID_5190
http://purl.obolibrary.org/obo/DOID_5190 EquivalentTo 'cervical wilms' tumor'
http://purl.obolibrary.org/obo/DOID_5190 EquivalentTo 'cervical wilms tumor'
http://purl.obolibrary.org/obo/MONDO_0009688
myasthenia gravis
'myasthenia gravis' SubClassOf 'autoimmune disease of peripheral nervous system'
'myasthenia gravis' SubClassOf 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/MONDO_0010688
neuropathy, hereditary sensory, X-linked
'neuropathy, hereditary sensory, X-linked' SubClassOf 'hereditary sensory and autonomic neuropathy'
http://purl.obolibrary.org/obo/DOID_0070159 EquivalentTo 'neuropathy, hereditary sensory, X-linked'
'neuropathy, hereditary sensory, X-linked' SubClassOf 'hereditary sensory and autonomic neuropathy'
http://purl.obolibrary.org/obo/MONDO_0009696
juvenile myoclonic epilepsy
'juvenile myoclonic epilepsy' SubClassOf 'childhood electroclinical syndrome'
'juvenile myoclonic epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100030
http://purl.obolibrary.org/obo/MONDO_0019013
non-histaminic angioedema
'non-histaminic angioedema' SubClassOf 'rare allergic disease'
'non-histaminic angioedema' SubClassOf 'allergic urticaria'
http://purl.obolibrary.org/obo/MONDO_0019053
peroxisomal disease
'peroxisomal disease' SubClassOf 'rare genetic epilepsy'
'peroxisomal disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/MONDO_0019046
leukodystrophy
http://purl.obolibrary.org/obo/DOID_0050987 EquivalentTo 'leukodystrophy'
http://purl.obolibrary.org/obo/MONDO_0020072
childhood-onset epilepsy syndrome
'childhood-onset epilepsy syndrome' EquivalentTo 'epilepsy syndrome' and ('has modifier' some http://purl.obolibrary.org/obo/HP_0011463)
'childhood-onset epilepsy syndrome' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/HP_0011463
http://purl.obolibrary.org/obo/MONDO_0020076
myeloproliferative neoplasm
'myeloproliferative neoplasm' SubClassOf 'rare immune disease'
'myeloproliferative neoplasm' SubClassOf 'rare bone disease'
http://purl.obolibrary.org/obo/MONDO_0020074
progressive myoclonic epilepsy
'progressive myoclonic epilepsy' SubClassOf 'childhood electroclinical syndrome'
http://purl.obolibrary.org/obo/MONDO_0019098
autoimmune thrombocytopenia
'autoimmune thrombocytopenia' EquivalentTo 'thrombocytopenia' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'autoimmune thrombocytopenia' EquivalentTo 'thrombocytopenia' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0020088
familial partial lipodystrophy
'familial partial lipodystrophy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0027767
'familial partial lipodystrophy' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0027767 and ('has modifier' some 'genetic')
http://purl.obolibrary.org/obo/MONDO_0009509
Landau-Kleffner syndrome
'Landau-Kleffner syndrome' SubClassOf 'childhood-onset epilepsy syndrome'
'Landau-Kleffner syndrome' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0009532
Miller-Dieker lissencephaly syndrome
'Miller-Dieker lissencephaly syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'Miller-Dieker lissencephaly syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0009571
Meckel syndrome, type 1
'Meckel syndrome, type 1' SubClassOf 'Meckel syndrome'
'Meckel syndrome, type 1' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070115 EquivalentTo 'Meckel syndrome, type 1'
http://purl.obolibrary.org/obo/MONDO_0010584
dyskeratosis congenita, X-linked
'dyskeratosis congenita, X-linked' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070025 EquivalentTo 'dyskeratosis congenita, X-linked'
'dyskeratosis congenita, X-linked' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/MONDO_0010583
Dyggve-Melchior-Clausen syndrome, X-linked
'Dyggve-Melchior-Clausen syndrome, X-linked' SubClassOf 'X-linked disease'
'Dyggve-Melchior-Clausen syndrome, X-linked' SubClassOf 'X-linked spondyloepimetaphyseal dysplasia'
http://purl.obolibrary.org/obo/MONDO_0010590
FG syndrome 1
'FG syndrome 1' SubClassOf 'MED12-related intellectual disability syndrome'
'FG syndrome 1' SubClassOf 'MED12-related intellectual disability syndrome'
http://www.orpha.net/ORDO/Orphanet_2190
'congenital hydronephrosis' EquivalentTo http://www.orpha.net/ORDO/Orphanet_2190
http://purl.obolibrary.org/obo/MONDO_0009411
autoimmune polyendocrine syndrome type 1
'autoimmune polyendocrine syndrome type 1' SubClassOf 'autoimmune hypoparathyroidism (disease)'
http://purl.obolibrary.org/obo/MONDO_0010475
X-linked central congenital hypothyroidism with late-onset testicular enlargement
'X-linked central congenital hypothyroidism with late-onset testicular enlargement' SubClassOf 'X-linked disease'
http://purl.obolibrary.org/obo/DOID_0111140 EquivalentTo 'X-linked central congenital hypothyroidism with late-onset testicular enlargement'
http://purl.obolibrary.org/obo/DOID_5709
http://purl.obolibrary.org/obo/DOID_5709 EquivalentTo 'mixed-type liposarcoma'
http://purl.obolibrary.org/obo/DOID_5709 EquivalentTo 'myxoid liposarcoma'
http://purl.obolibrary.org/obo/MONDO_0000974
axillary lipoma
'axillary lipoma' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0009472
'axillary lipoma' SubClassOf 'thoracic benign neoplasm'
'axillary lipoma' EquivalentTo 'lipoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0009472)
'axillary lipoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036781
'axillary lipoma' EquivalentTo 'lipoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0009472)
http://purl.obolibrary.org/obo/MONDO_0009303
anti-glomerular basement membrane disease
'anti-glomerular basement membrane disease' SubClassOf 'rare immune disease'
'anti-glomerular basement membrane disease' SubClassOf 'autoimmune disease of cardiovascular system'
'anti-glomerular basement membrane disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_0030703
http://purl.obolibrary.org/obo/MONDO_0000994
malignant prostate phyllodes tumor
'malignant prostate phyllodes tumor' SubClassOf 'malignant mixed neoplasm'
'malignant prostate phyllodes tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037003
http://purl.obolibrary.org/obo/MONDO_0010375
hyperekplexia-epilepsy syndrome
'hyperekplexia-epilepsy syndrome' SubClassOf 'early infantile epileptic encephalopathy'
'hyperekplexia-epilepsy syndrome' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/DOID_0080215 EquivalentTo 'hyperekplexia-epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0000805
snail allergy
'snail allergy' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00002244)
'snail allergy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00002244
http://purl.obolibrary.org/obo/MONDO_0000870
childhood acute lymphoblastic leukemia
'childhood acute lymphoblastic leukemia' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0000874
T-cell childhood lymphoblastic lymphoma
'T-cell childhood lymphoblastic lymphoma' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0010204
lysosomal acid lipase deficiency
'lysosomal acid lipase deficiency' SubClassOf 'lipid storage disorder'
http://purl.obolibrary.org/obo/DOID_0080217 EquivalentTo 'lysosomal acid lipase deficiency'
'lysosomal acid lipase deficiency' SubClassOf 'lipid storage disorder'
http://purl.obolibrary.org/obo/MONDO_0000894
mucinous bronchioloalveolar adenocarcinoma
'mucinous bronchioloalveolar adenocarcinoma' SubClassOf 'mucinous adenocarcinoma'
'mucinous bronchioloalveolar adenocarcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0027772
http://purl.obolibrary.org/obo/MONDO_0024884
metastatic carcinoma in the bone
'metastatic carcinoma in the bone' SubClassOf 'bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0024885
malignant ovarian serous tumor
'malignant ovarian serous tumor' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037255 and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
'malignant ovarian serous tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037255
http://purl.obolibrary.org/obo/MONDO_0024889
benign mesonephroma
'benign mesonephroma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0000774
autoimmune neuropathy
'autoimmune neuropathy' SubClassOf 'autoimmune disease of peripheral nervous system'
http://purl.obolibrary.org/obo/DOID_0040087 EquivalentTo 'autoimmune neuropathy'
'autoimmune neuropathy' EquivalentTo 'peripheral neuropathy' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune neuropathy' SubClassOf 'peripheral neuropathy'
http://purl.obolibrary.org/obo/MONDO_0000798
mollusc allergy
'mollusc allergy' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00002044)
'mollusc allergy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00002044
http://purl.obolibrary.org/obo/MONDO_0000797
goat milk allergy
'goat milk allergy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00001911
'goat milk allergy' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00001911)
http://purl.obolibrary.org/obo/MONDO_0000796
cow milk allergy (disease)
'cow milk allergy (disease)' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00001771
'cow milk allergy (disease)' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00001771)
http://purl.obolibrary.org/obo/MONDO_0009126
duodenal atresia (disease)
'duodenal atresia (disease)' SubClassOf 'rare genetic intestinal disease'
'duodenal atresia (disease)' SubClassOf 'intestinal atresia (disease)'
http://purl.obolibrary.org/obo/DOID_0080216 EquivalentTo 'duodenal atresia (disease)'
http://purl.obolibrary.org/obo/MONDO_0009130
Dyggve-Melchior-Clausen disease
http://purl.obolibrary.org/obo/DOID_0111167 EquivalentTo 'Dyggve-Melchior-Clausen disease'
'Dyggve-Melchior-Clausen disease' SubClassOf 'spondyloepimetaphyseal dysplasia'
http://purl.obolibrary.org/obo/MONDO_0000799
crustacean allergy
'crustacean allergy' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00001792)
'crustacean allergy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00001792
http://purl.obolibrary.org/obo/MONDO_0009136
dyskeratosis congenita, autosomal recessive 1
'dyskeratosis congenita, autosomal recessive 1' SubClassOf 'dyskeratosis congenita'
'dyskeratosis congenita, autosomal recessive 1' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070015 EquivalentTo 'dyskeratosis congenita, autosomal recessive 1'
http://purl.obolibrary.org/obo/MONDO_0010139
isolated thyroid-stimulating hormone deficiency
http://purl.obolibrary.org/obo/DOID_0070123 EquivalentTo 'isolated thyroid-stimulating hormone deficiency'
http://purl.obolibrary.org/obo/MONDO_0009152
ectopia lentis 2, isolated, autosomal recessive
http://purl.obolibrary.org/obo/DOID_0111149 EquivalentTo 'ectopia lentis 2, isolated, autosomal recessive'
http://purl.obolibrary.org/obo/MONDO_0009154
hypothyroidism, congenital, Nongoitrous, 5
http://purl.obolibrary.org/obo/DOID_0070125 EquivalentTo 'hypothyroidism, congenital, Nongoitrous, 5'
http://purl.obolibrary.org/obo/MONDO_0010142
hypothyroidism due to TSH receptor mutations
http://purl.obolibrary.org/obo/DOID_0070126 EquivalentTo 'hypothyroidism due to TSH receptor mutations'
http://purl.obolibrary.org/obo/MONDO_0009187
celiac disease-epilepsy-cerebral calcification syndrome
'celiac disease-epilepsy-cerebral calcification syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100029
http://purl.obolibrary.org/obo/MONDO_0005405
childhood onset asthma
'childhood onset asthma' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/HP_0011463
'childhood onset asthma' EquivalentTo 'asthma' and ('has modifier' some http://purl.obolibrary.org/obo/HP_0011463)
http://purl.obolibrary.org/obo/OMIM_133200
'erythrokeratodermia variabilis' EquivalentTo http://purl.obolibrary.org/obo/OMIM_133200
http://purl.obolibrary.org/obo/MONDO_0033010 EquivalentTo http://purl.obolibrary.org/obo/OMIM_133200
http://purl.obolibrary.org/obo/MONDO_0019933
acromegaly
'acromegaly' SubClassOf 'benign reproductive system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0019941
hereditary sensory and autonomic neuropathy type 2
http://purl.obolibrary.org/obo/DOID_0070161 EquivalentTo 'hereditary sensory and autonomic neuropathy type 2'
http://purl.obolibrary.org/obo/MONDO_0019972
dural sinus malformation
'dural sinus malformation' SubClassOf 'nervous system benign neoplasm'
'dural sinus malformation' SubClassOf 'intracranial hemangioma'
http://purl.obolibrary.org/obo/MONDO_0005210
uterine corpus sarcoma
'uterine corpus sarcoma' SubClassOf 'uterine corpus cancer'
http://purl.obolibrary.org/obo/MONDO_0005229
bacteriemia
http://purl.obolibrary.org/obo/DOID_0040085 EquivalentTo 'bacteriemia'
'bacteriemia' EquivalentTo 'bacterial infectious disease' and ('disease has feature' some http://purl.obolibrary.org/obo/HP_0100806)
http://purl.obolibrary.org/obo/MONDO_0005238
round cell liposarcoma
'round cell liposarcoma' SubClassOf 'liposarcoma'
'round cell liposarcoma' SubClassOf 'myxoid/round cell liposarcoma'
http://purl.obolibrary.org/obo/MONDO_0005249
pneumonia
http://purl.obolibrary.org/obo/ICD10_J15 EquivalentTo 'pneumonia'
http://purl.obolibrary.org/obo/MONDO_0005271
allergic disease
'allergic disease' EquivalentTo 'immune system disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0016068)
'allergic disease' SubClassOf 'hypersensitivity reaction disease'
'allergic disease' EquivalentTo 'disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0016068)
'allergic disease' SubClassOf 'hypersensitivity reaction disease'
http://linkedlifedata.com/resource/umls/id/C1527304 EquivalentTo 'allergic disease'
'allergic disease' DisjointWith 'hypersensitivity reaction type II disease'
http://purl.obolibrary.org/obo/MONDO_0019719
renal or urinary tract malformation
http://purl.obolibrary.org/obo/DOID_0080205 EquivalentTo 'renal or urinary tract malformation'
http://purl.obolibrary.org/obo/MONDO_0005100
systemic sclerosis
'systemic sclerosis' SubClassOf 'autoimmune disease of cardiovascular system'
'systemic sclerosis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0030701
http://purl.obolibrary.org/obo/MONDO_0019754
multicentric Castleman disease
http://purl.obolibrary.org/obo/DOID_0111152 EquivalentTo 'multicentric Castleman disease'
http://purl.obolibrary.org/obo/MONDO_0005183
ovarian cystadenoma
'ovarian cystadenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0019609
Zellweger syndrome
'Zellweger syndrome' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0019606
simple cryoglobulinemia
'simple cryoglobulinemia' SubClassOf 'autoimmune disease of peripheral nervous system'
'simple cryoglobulinemia' SubClassOf 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/MONDO_0019615
pituitary dermoid and epidermoid cysts
'pituitary dermoid and epidermoid cysts' SubClassOf 'rare nervous system tumor'
'pituitary dermoid and epidermoid cysts' SubClassOf 'brain neoplasm'
'pituitary dermoid and epidermoid cysts' SubClassOf 'pituitary tumor'
http://purl.obolibrary.org/obo/MONDO_0019637
renal hypoplasia (disease)
http://purl.obolibrary.org/obo/DOID_0080204 EquivalentTo 'renal hypoplasia (disease)'
http://purl.obolibrary.org/obo/MONDO_0005029
essential thrombocythemia
'essential thrombocythemia' SubClassOf 'rare vascular tumor'
'essential thrombocythemia' SubClassOf 'vascular bone neoplasm'
http://purl.obolibrary.org/obo/MONDO_0005032
follicular thyroid adenoma
'follicular thyroid adenoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036976
http://purl.obolibrary.org/obo/MONDO_0005098
stroke
'stroke' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/MONDO_0020539
extragonadal non-dysgerminomatous germ cell tumor
'extragonadal non-dysgerminomatous germ cell tumor' EquivalentTo 'extragonadal germ cell tumor' and 'nongerminomatous germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0019536
typical hemolytic-uremic syndrome
'typical hemolytic-uremic syndrome' SubClassOf 'acquired metabolic disease'
http://purl.obolibrary.org/obo/MONDO_0020542
malignant Sertoli-leydig cell tumor of ovary
'malignant Sertoli-leydig cell tumor of ovary' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036595
'malignant Sertoli-leydig cell tumor of ovary' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0036595 and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
http://purl.obolibrary.org/obo/MONDO_0019563
CREST syndrome
'CREST syndrome' SubClassOf 'autoimmune disease of peripheral nervous system'
'CREST syndrome' SubClassOf 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/MONDO_0019572
autosomal recessive cutis laxa type 1
'autosomal recessive cutis laxa type 1' SubClassOf 'cutis laxa'
http://purl.obolibrary.org/obo/DOID_0070144 EquivalentTo 'autosomal recessive cutis laxa type 1'
'autosomal recessive cutis laxa type 1' SubClassOf 'cutis laxa'
http://purl.obolibrary.org/obo/MONDO_0019571
autosomal dominant cutis laxa
'autosomal dominant cutis laxa' SubClassOf 'cutis laxa'
http://purl.obolibrary.org/obo/DOID_0070142 EquivalentTo 'autosomal dominant cutis laxa'
'autosomal dominant cutis laxa' SubClassOf 'cutis laxa'
http://purl.obolibrary.org/obo/MONDO_0019471
adult T-cell leukemia/lymphoma
'adult T-cell leukemia/lymphoma' SubClassOf 'rare genetic bone disease'
'adult T-cell leukemia/lymphoma' SubClassOf 'inherited syndrome with bone tumors as a major feature'
'adult T-cell leukemia/lymphoma' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0019465
nodal marginal zone B-cell lymphoma
'nodal marginal zone B-cell lymphoma' SubClassOf 'marginal zone lymphoma'
http://purl.obolibrary.org/obo/DOID_0080211 EquivalentTo 'nodal marginal zone B-cell lymphoma'
'nodal marginal zone B-cell lymphoma' SubClassOf 'marginal zone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0019464
heavy chain disease
'heavy chain disease' SubClassOf 'autoimmune disease of blood'
http://purl.obolibrary.org/obo/MONDO_0020460
acquired von willebrand syndrome
http://purl.obolibrary.org/obo/DOID_0111146 EquivalentTo 'acquired von willebrand syndrome'
http://purl.obolibrary.org/obo/MONDO_0019487
epilepsy with myoclonic absences
'epilepsy with myoclonic absences' SubClassOf 'childhood-onset epilepsy syndrome'
'epilepsy with myoclonic absences' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0019486
myoclonic epilepsy of infancy
'myoclonic epilepsy of infancy' SubClassOf 'infantile epilepsy syndrome'
'myoclonic epilepsy of infancy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100022
http://purl.obolibrary.org/obo/MONDO_0020491
subcortical band heterotopia
'subcortical band heterotopia' SubClassOf 'congenital nervous system abnormality'
http://purl.obolibrary.org/obo/DOID_0111169 EquivalentTo 'subcortical band heterotopia'
http://purl.obolibrary.org/obo/MONDO_0020480
sulfite oxidase deficiency due to molybdenum cofactor deficiency
'sulfite oxidase deficiency due to molybdenum cofactor deficiency' SubClassOf 'inborn metal metabolism disorder'
http://purl.obolibrary.org/obo/DOID_0111165 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency'
http://purl.obolibrary.org/obo/MONDO_0009919
peroxisomal acyl-CoA oxidase deficiency
'peroxisomal acyl-CoA oxidase deficiency' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0010911
prolactin-producing pituitary gland adenoma
'prolactin-producing pituitary gland adenoma' SubClassOf 'benign male reproductive system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0009945
pyridoxine-dependent epilepsy
'pyridoxine-dependent epilepsy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100033
http://purl.obolibrary.org/obo/MONDO_0010943
schizophrenia 4
'schizophrenia 4' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070080 EquivalentTo 'schizophrenia 4'
'schizophrenia 4' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0009966
NPHP3-related Meckel-like syndrome
'NPHP3-related Meckel-like syndrome' SubClassOf 'Meckel syndrome'
'NPHP3-related Meckel-like syndrome' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070121 EquivalentTo 'NPHP3-related Meckel-like syndrome'
http://purl.obolibrary.org/obo/MONDO_0020310
familial focal epilepsy with variable foci
'familial focal epilepsy with variable foci' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100036
http://purl.obolibrary.org/obo/MONDO_0009990
Revesz syndrome
'Revesz syndrome' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/DOID_0070026 EquivalentTo 'Revesz syndrome'
'Revesz syndrome' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/MONDO_0020323
primary mediastinal large B-cell lymphoma
'primary mediastinal large B-cell lymphoma' SubClassOf 'diffuse large B-cell lymphoma'
'primary mediastinal large B-cell lymphoma' SubClassOf 'diffuse large B-cell lymphoma'
http://purl.obolibrary.org/obo/DOID_0080210 EquivalentTo 'primary mediastinal large B-cell lymphoma'
http://purl.obolibrary.org/obo/MONDO_0020349
acute motor axonal neuropathy
'acute motor axonal neuropathy' SubClassOf 'autoimmune disease of central nervous system'
http://purl.obolibrary.org/obo/MONDO_0020348
acute motor and sensory axonal neuropathy
'acute motor and sensory axonal neuropathy' SubClassOf 'autoimmune disease of central nervous system'
http://purl.obolibrary.org/obo/MONDO_0020347
acute inflammatory demyelinating polyradiculoneuropathy
'acute inflammatory demyelinating polyradiculoneuropathy' SubClassOf 'autoimmune disease of central nervous system'
http://purl.obolibrary.org/obo/MONDO_0019385
steroid-responsive encephalopathy associated with autoimmune thyroiditis
'steroid-responsive encephalopathy associated with autoimmune thyroiditis' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100029
'steroid-responsive encephalopathy associated with autoimmune thyroiditis' SubClassOf 'rare epilepsy'
http://purl.obolibrary.org/obo/OMIM_251300
'Galloway-Mowat syndrome' EquivalentTo http://purl.obolibrary.org/obo/OMIM_251300
http://purl.obolibrary.org/obo/MONDO_0033005 EquivalentTo http://purl.obolibrary.org/obo/OMIM_251300
http://purl.obolibrary.org/obo/MONDO_0001052
chronic fungal otitis externa
'chronic fungal otitis externa' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic fungal otitis externa' EquivalentTo 'otomycosis' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
http://purl.obolibrary.org/obo/OMIM_143400
'congenital hydronephrosis' EquivalentTo http://purl.obolibrary.org/obo/OMIM_143400
http://purl.obolibrary.org/obo/MONDO_0027676 EquivalentTo http://purl.obolibrary.org/obo/OMIM_143400
http://purl.obolibrary.org/obo/MONDO_0015723
trisomy 12p
'trisomy 12p' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0015746
male infertility due to globozoospermia
'male infertility due to globozoospermia' SubClassOf 'disease arises from feature' some http://purl.obolibrary.org/obo/HP_0012205
http://purl.obolibrary.org/obo/DOID_0111156 EquivalentTo 'male infertility due to globozoospermia'
'male infertility due to globozoospermia' EquivalentTo 'male infertility' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0012205)
http://purl.obolibrary.org/obo/MONDO_0001123
chronic sphenoidal sinusitis
'chronic sphenoidal sinusitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic sphenoidal sinusitis' SubClassOf 'chronic rhinosinusitis'
http://purl.obolibrary.org/obo/MONDO_0001122
chronic maxillary sinusitis
'chronic maxillary sinusitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic maxillary sinusitis' SubClassOf 'chronic rhinosinusitis'
http://purl.obolibrary.org/obo/MONDO_0001120
chronic frontal sinusitis
'chronic frontal sinusitis' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic frontal sinusitis' SubClassOf 'chronic rhinosinusitis'
http://purl.obolibrary.org/obo/MONDO_0015564
Castleman disease
'Castleman disease' SubClassOf 'lymphoproliferative syndrome'
'Castleman disease' SubClassOf 'rare genetic hematologic disease'
http://purl.obolibrary.org/obo/DOID_0111157 EquivalentTo 'Castleman disease'
'Castleman disease' SubClassOf 'rare genetic inherited tumor'
http://purl.obolibrary.org/obo/MONDO_0015436
ring chromosome 20
'ring chromosome 20' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'ring chromosome 20' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0015448
isolated CoQ-cytochrome c reductase deficiency
'isolated CoQ-cytochrome c reductase deficiency' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/GO_0005750
'isolated CoQ-cytochrome c reductase deficiency' EquivalentTo 'disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/GO_0005750)
http://purl.obolibrary.org/obo/DOID_0111139 EquivalentTo 'isolated CoQ-cytochrome c reductase deficiency'
http://purl.obolibrary.org/obo/MONDO_0005972
streptococcal pneumonia
'streptococcal pneumonia' SubClassOf 'bacterial pneumonia'
http://purl.obolibrary.org/obo/DOID_0040084 EquivalentTo 'streptococcal pneumonia'
'streptococcal pneumonia' SubClassOf 'bacterial pneumonia'
http://purl.obolibrary.org/obo/MONDO_0015306
Lemierre syndrome
'Lemierre syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0100806
'Lemierre syndrome' SubClassOf 'bacteriemia'
http://purl.obolibrary.org/obo/MONDO_0005993
trichomonas vaginitis
'trichomonas vaginitis' SubClassOf 'trichomoniasis'
'trichomonas vaginitis' EquivalentTo 'disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
'trichomonas vaginitis' SubClassOf 'trichomoniasis'
http://purl.obolibrary.org/obo/DOID_0050269 EquivalentTo 'trichomonas vaginitis'
'trichomonas vaginitis' SubClassOf 'sexually transmitted disease'
'trichomonas vaginitis' SubClassOf 'disease of genitourinary system'
http://purl.obolibrary.org/obo/ICD10_A59.0 EquivalentTo 'trichomonas vaginitis'
'trichomonas vaginitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_35089004
'trichomonas vaginitis' SubClassOf 'disease has feature' some 'vaginal discharge'
'trichomonas vaginitis' EquivalentTo 'disease of genitourinary system' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
http://purl.obolibrary.org/obo/MONDO_0015340
drug rash with eosinophilia and systemic symptoms
'drug rash with eosinophilia and systemic symptoms' SubClassOf 'rare genetic immune disease'
http://purl.obolibrary.org/obo/MONDO_0015405
cerebrofacial arteriovenous metameric syndrome
'cerebrofacial arteriovenous metameric syndrome' SubClassOf 'nervous system benign neoplasm'
'cerebrofacial arteriovenous metameric syndrome' SubClassOf 'intracranial hemangioma'
http://purl.obolibrary.org/obo/MONDO_0005851
Miller Fisher syndrome
'Miller Fisher syndrome' SubClassOf 'autoimmune disease of central nervous system'
http://purl.obolibrary.org/obo/MONDO_0005854
mixed connective tissue disease
'mixed connective tissue disease' SubClassOf 'autoimmune disease of peripheral nervous system'
'mixed connective tissue disease' SubClassOf 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/MONDO_0005867
Mycoplasma pneumoniae pneumonia
'Mycoplasma pneumoniae pneumonia' SubClassOf 'pneumonia'
'Mycoplasma pneumoniae pneumonia' SubClassOf 'bacterial pneumonia'
http://purl.obolibrary.org/obo/DOID_13276 EquivalentTo 'Mycoplasma pneumoniae pneumonia'
http://purl.obolibrary.org/obo/MONDO_0005872
nervous system cancer
'nervous system cancer' SubClassOf 'nervous system neoplasm'
'nervous system cancer' SubClassOf 'nervous system neoplasm'
'nervous system cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4788
http://purl.obolibrary.org/obo/MONDO_0005945
rhinoscleroma
'rhinoscleroma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0030603
http://purl.obolibrary.org/obo/MONDO_0005966
spleen cancer
'spleen cancer' SubClassOf 'splenic disease'
'spleen cancer' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036696
http://purl.obolibrary.org/obo/MONDO_0005754
epilepsy with generalized tonic-clonic seizures
'epilepsy with generalized tonic-clonic seizures' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100030
http://purl.obolibrary.org/obo/MONDO_0005767
gas gangrene
'gas gangrene' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0100806
'gas gangrene' SubClassOf 'bacteriemia'
http://purl.obolibrary.org/obo/MONDO_0005769
geniculate herpes zoster
'geniculate herpes zoster' SubClassOf 'rare otorhinolaryngologic disease'
'geniculate herpes zoster' SubClassOf 'infectious disease of the nervous system'
http://purl.obolibrary.org/obo/MONDO_0005777
granuloma inguinale
'granuloma inguinale' SubClassOf http://purl.obolibrary.org/obo/MONDO_0030603
http://purl.obolibrary.org/obo/MONDO_0015145
neurovascular malformation
'neurovascular malformation' SubClassOf 'rare epilepsy'
'neurovascular malformation' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/MONDO_0015169
chronic diarrhea due to glucoamylase deficiency
'chronic diarrhea due to glucoamylase deficiency' EquivalentTo 'diarrhea (disease)' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0004339)
'chronic diarrhea due to glucoamylase deficiency' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0004339
'chronic diarrhea due to glucoamylase deficiency' SubClassOf 'diarrhea (disease)'
'chronic diarrhea due to glucoamylase deficiency' SubClassOf 'disease disrupting molecular activity'
http://purl.obolibrary.org/obo/MONDO_0015175
autoimmune pancreatitis
'autoimmune pancreatitis' SubClassOf 'autoimmune disease of endocrine system'
'autoimmune pancreatitis' SubClassOf 'autoimmune disease of endocrine system'
'autoimmune pancreatitis' EquivalentTo 'pancreatitis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune pancreatitis' SubClassOf 'pancreatitis'
http://purl.obolibrary.org/obo/DOID_0040091 EquivalentTo 'autoimmune pancreatitis'
http://purl.obolibrary.org/obo/MONDO_0005616
pulmonary mucoepidermoid carcinoma
'pulmonary mucoepidermoid carcinoma' SubClassOf 'lung adenocarcinoma'
'pulmonary mucoepidermoid carcinoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0027772
http://purl.obolibrary.org/obo/MONDO_0005642
atopic conjunctivitis
'atopic conjunctivitis' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0016068
'atopic conjunctivitis' SubClassOf 'eye allergy'
http://purl.obolibrary.org/obo/MONDO_0015079
multiple polyglandular tumor
'multiple polyglandular tumor' SubClassOf 'rare genetic inherited tumor'
'multiple polyglandular tumor' SubClassOf 'rare genetic endocrine disease'
http://purl.obolibrary.org/obo/MONDO_0005505
dysembryoplastic neuroepithelial tumor
'dysembryoplastic neuroepithelial tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
'dysembryoplastic neuroepithelial tumor' SubClassOf 'rare epilepsy'
http://purl.obolibrary.org/obo/MONDO_0005507
gingival cancer
'gingival cancer' SubClassOf 'rare odontologic tumor'
'gingival cancer' SubClassOf 'rare gastroenterologic disease'
http://purl.obolibrary.org/obo/MONDO_0005544
hippocampal sclerosis of aging
'hippocampal sclerosis of aging' SubClassOf 'brain disease'
'hippocampal sclerosis of aging' SubClassOf http://purl.obolibrary.org/obo/MONDO_0100035
http://purl.obolibrary.org/obo/MONDO_0005576
cryoglobulinemia
'cryoglobulinemia' SubClassOf 'hypersensitivity reaction type II disease'
http://purl.obolibrary.org/obo/MONDO_0011296
Meckel syndrome, type 2
'Meckel syndrome, type 2' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/DOID_0070116 EquivalentTo 'Meckel syndrome, type 2'
'Meckel syndrome, type 2' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/MONDO_0011298
SCZD8
'SCZD8' SubClassOf 'schizophrenia (disease)'
'SCZD8' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070084 EquivalentTo 'SCZD8'
http://purl.obolibrary.org/obo/MONDO_0011295
SCZD7
'SCZD7' SubClassOf 'schizophrenia (disease)'
'SCZD7' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070083 EquivalentTo 'SCZD7'
http://purl.obolibrary.org/obo/MONDO_0011294
SCZD5
'SCZD5' SubClassOf 'schizophrenia (disease)'
'SCZD5' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070081 EquivalentTo 'SCZD5'
http://purl.obolibrary.org/obo/MONDO_0011307
SCZD2
'SCZD2' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070078 EquivalentTo 'SCZD2'
'SCZD2' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0011301
pseudohypoparathyroidism type 1B
http://purl.obolibrary.org/obo/DOID_0080222 EquivalentTo 'pseudohypoparathyroidism type 1B'
http://purl.obolibrary.org/obo/MONDO_0001995
sphenoid sinus squamous cell carcinoma
'sphenoid sinus squamous cell carcinoma' SubClassOf 'rare bone disease'
'sphenoid sinus squamous cell carcinoma' SubClassOf 'rare respiratory disease'
'sphenoid sinus squamous cell carcinoma' SubClassOf 'rare nervous system tumor'
'sphenoid sinus squamous cell carcinoma' SubClassOf 'bone squamous cell carcinoma'
http://purl.obolibrary.org/obo/MONDO_0011280
SCZD6
'SCZD6' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/DOID_0070082 EquivalentTo 'SCZD6'
'SCZD6' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0001743
paranasal sinus lymphoma
'paranasal sinus lymphoma' SubClassOf 'rare bone disease'
'paranasal sinus lymphoma' SubClassOf 'lymphoma'
'paranasal sinus lymphoma' SubClassOf 'rare nervous system tumor'
'paranasal sinus lymphoma' SubClassOf 'rare head and neck tumor'
'paranasal sinus lymphoma' SubClassOf 'rare respiratory disease'
'paranasal sinus lymphoma' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0001758
paranasal sinus sarcoma
'paranasal sinus sarcoma' SubClassOf 'rare nervous system tumor'
'paranasal sinus sarcoma' SubClassOf 'rare bone disease'
'paranasal sinus sarcoma' SubClassOf 'rare respiratory disease'
'paranasal sinus sarcoma' SubClassOf 'rare head and neck tumor'
http://purl.obolibrary.org/obo/MONDO_0011147
chromosome 18q deletion syndrome
'chromosome 18q deletion syndrome' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/MONDO_0011146
tetrasomy 12p
'tetrasomy 12p' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
'tetrasomy 12p' SubClassOf 'chromosomal anomaly with epilepsy as a major feature'
http://purl.obolibrary.org/obo/SCTID_127024001
'pituitary cancer' EquivalentTo http://purl.obolibrary.org/obo/SCTID_127024001
'pituitary tumor' EquivalentTo http://purl.obolibrary.org/obo/SCTID_127024001
http://purl.obolibrary.org/obo/MONDO_0001607
intrapelvic lymph node leukemic reticuloendotheliosis
'intrapelvic lymph node leukemic reticuloendotheliosis' SubClassOf 'primary bone lymphoma'
http://purl.obolibrary.org/obo/MONDO_0001606
central nervous system leukemia
'central nervous system leukemia' SubClassOf 'bone marrow cancer'
http://purl.obolibrary.org/obo/MONDO_0001691
laryngeal cartilage cancer
'laryngeal cartilage cancer' SubClassOf 'rare respiratory disease'
http://purl.obolibrary.org/obo/MONDO_0011014
pleuropulmonary blastoma
'pleuropulmonary blastoma' SubClassOf 'childhood malignant neoplasm'
'pleuropulmonary blastoma' SubClassOf http://purl.obolibrary.org/obo/MONDO_0036491
http://purl.obolibrary.org/obo/MONDO_0025485
feline acquired immunodeficiency syndrome
'feline acquired immunodeficiency syndrome' EquivalentTo 'cat disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11673)
http://purl.obolibrary.org/obo/MONDO_0025484
simian acquired immunodeficiency syndrome
'simian acquired immunodeficiency syndrome' EquivalentTo 'monkey disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11723)
http://purl.obolibrary.org/obo/MONDO_0001580
lacrimal duct cancer
'lacrimal duct cancer' SubClassOf 'lacrimal apparatus disease'
http://purl.obolibrary.org/obo/MONDO_0001438
postinflammatory pulmonary fibrosis
'postinflammatory pulmonary fibrosis' SubClassOf 'disease arises from feature' some 'inflammatory disease'
'postinflammatory pulmonary fibrosis' EquivalentTo 'pulmonary fibrosis' and ('disease arises from feature' some 'inflammatory disease')
http://purl.obolibrary.org/obo/MONDO_0001458
ulnar nerve lesion
'ulnar nerve lesion' SubClassOf 'disorder of anatomical region'
'ulnar nerve lesion' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0001494
'ulnar nerve lesion' SubClassOf 'brachial plexus neuropathy'
http://purl.obolibrary.org/obo/MONDO_0001482
testicular leukemia
'testicular leukemia' SubClassOf 'rare endocrine disease'
http://purl.obolibrary.org/obo/MONDO_0001251
chronic apical periodontitis
'chronic apical periodontitis' SubClassOf 'chronic periodontitis'
'chronic apical periodontitis' EquivalentTo 'periapical periodontitis' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
http://purl.obolibrary.org/obo/MONDO_0001290
allergic cutaneous vasculitis
'allergic cutaneous vasculitis' SubClassOf 'vasculitis'
'allergic cutaneous vasculitis' SubClassOf 'skin vascular disease'
http://purl.obolibrary.org/obo/MONDO_0015939
systemic autoimmune disease
'systemic autoimmune disease' EquivalentTo 'systemic disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'systemic autoimmune disease' EquivalentTo 'systemic disease' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/MONDO_0015998
isolated ectopia lentis
http://purl.obolibrary.org/obo/DOID_0111148 EquivalentTo 'isolated ectopia lentis'
'isolated ectopia lentis' SubClassOf 'lens disease'
http://purl.obolibrary.org/obo/MONDO_0001367
chronic congestive splenomegaly
'chronic congestive splenomegaly' SubClassOf 'splenic disease'
'chronic congestive splenomegaly' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/PATO_0001863
'chronic congestive splenomegaly' EquivalentTo http://purl.obolibrary.org/obo/MONDO_0037251 and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
'chronic congestive splenomegaly' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037251
http://purl.obolibrary.org/obo/MONDO_0015776
rhizomelic chondrodysplasia punctata
'rhizomelic chondrodysplasia punctata' SubClassOf 'rare genetic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0001227
chronic tympanitis
http://purl.obolibrary.org/obo/COHD_372652 EquivalentTo 'chronic tympanitis'
'chronic tympanitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_89723004
'chronic tympanitis' SubClassOf 'tympanitis'
http://linkedlifedata.com/resource/umls/id/C0395849 EquivalentTo 'chronic tympanitis'
http://purl.obolibrary.org/obo/DOID_11217 EquivalentTo 'chronic tympanitis'
http://purl.obolibrary.org/obo/MONDO_0015864
mixed germ cell tumor
'mixed germ cell tumor' SubClassOf 'extragonadal non-dysgerminomatous germ cell tumor'
'mixed germ cell tumor' SubClassOf 'extragonadal germ cell cancer'
'mixed germ cell tumor' SubClassOf 'malignant germ cell tumor'
http://purl.obolibrary.org/obo/DOID_3306 EquivalentTo 'mixed germ cell tumor'
http://purl.obolibrary.org/obo/MONDO_0015871
benign breast phyllodes tumor
'benign breast phyllodes tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_0037002
http://purl.obolibrary.org/obo/UBERON_0002337
http://purl.obolibrary.org/obo/UBERON_0002337 SubClassOf http://purl.obolibrary.org/obo/CARO_0000003
http://purl.obolibrary.org/obo/NCIT_C35176
'trichomonas prostatitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35176
http://purl.obolibrary.org/obo/SCTID_92047003
'benign neoplasm of cauda equina' EquivalentTo http://purl.obolibrary.org/obo/SCTID_92047003
http://purl.obolibrary.org/obo/ICD10_A59.0
http://purl.obolibrary.org/obo/ICD10_A59.0 EquivalentTo 'trichomonas vaginitis urogenital infection'
http://purl.obolibrary.org/obo/NCIT_C6897
'cystic partially differentiated nephroblastoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6897
http://purl.obolibrary.org/obo/DOID_0050756
http://purl.obolibrary.org/obo/DOID_0050756 EquivalentTo 'juvenile neuronal ceroid lipofuscinosis'
http://purl.obolibrary.org/obo/DOID_0050987
http://purl.obolibrary.org/obo/DOID_0050987 EquivalentTo 'leukodystrophy'
http://purl.obolibrary.org/obo/DOID_0070029
http://purl.obolibrary.org/obo/DOID_0070029 EquivalentTo 'ABri amyloidosis'
http://purl.obolibrary.org/obo/DOID_0070027
http://purl.obolibrary.org/obo/DOID_0070027 EquivalentTo 'ACys amyloidosis'
http://purl.obolibrary.org/obo/DOID_0070028
http://purl.obolibrary.org/obo/DOID_0070028 EquivalentTo 'cerebral amyloid angiopathy, App-related'
http://purl.obolibrary.org/obo/DOID_0070025
http://purl.obolibrary.org/obo/DOID_0070025 EquivalentTo 'dyskeratosis congenita, X-linked'
http://purl.obolibrary.org/obo/DOID_0070026
http://purl.obolibrary.org/obo/DOID_0070026 EquivalentTo 'Revesz syndrome'
http://purl.obolibrary.org/obo/DOID_0070023
http://purl.obolibrary.org/obo/DOID_0070023 EquivalentTo 'dyskeratosis congenita, autosomal dominant 6'
http://purl.obolibrary.org/obo/DOID_0070024
http://purl.obolibrary.org/obo/DOID_0070024 EquivalentTo 'dyskeratosis congenita, autosomal recessive 6'
http://purl.obolibrary.org/obo/DOID_0070032
http://purl.obolibrary.org/obo/DOID_0070032 EquivalentTo 'intellectual disability, autosomal dominant 2'
http://purl.obolibrary.org/obo/DOID_0070033
http://purl.obolibrary.org/obo/DOID_0070033 EquivalentTo 'intellectual disability, autosomal dominant 3'
http://purl.obolibrary.org/obo/DOID_0070030
http://purl.obolibrary.org/obo/DOID_0070030 EquivalentTo 'ADan amyloidosis'
http://purl.obolibrary.org/obo/DOID_0070031
http://purl.obolibrary.org/obo/DOID_0070031 EquivalentTo 'intellectual disability, autosomal dominant 1'
http://purl.obolibrary.org/obo/DOID_0070038
http://purl.obolibrary.org/obo/DOID_0070038 EquivalentTo 'intellectual disability, autosomal dominant 8'
http://purl.obolibrary.org/obo/DOID_0070039
http://purl.obolibrary.org/obo/DOID_0070039 EquivalentTo 'intellectual disability, autosomal dominant 9'
http://purl.obolibrary.org/obo/DOID_0070036
http://purl.obolibrary.org/obo/DOID_0070036 EquivalentTo 'intellectual disability, autosomal dominant 6'
http://purl.obolibrary.org/obo/DOID_0070037
http://purl.obolibrary.org/obo/DOID_0070037 EquivalentTo 'DYRK1A-related intellectual disability syndrome'
http://purl.obolibrary.org/obo/DOID_0070034
http://purl.obolibrary.org/obo/DOID_0070034 EquivalentTo 'intellectual disability, autosomal dominant 4'
http://purl.obolibrary.org/obo/DOID_0070035
http://purl.obolibrary.org/obo/DOID_0070035 EquivalentTo 'intellectual disability, autosomal dominant 5'
http://purl.obolibrary.org/obo/DOID_0070043
http://purl.obolibrary.org/obo/DOID_0070043 EquivalentTo 'intellectual disability, autosomal dominant 13'
http://purl.obolibrary.org/obo/DOID_0070044
http://purl.obolibrary.org/obo/DOID_0070044 EquivalentTo 'intellectual disability, autosomal dominant 14'
http://purl.obolibrary.org/obo/DOID_0070041
http://purl.obolibrary.org/obo/DOID_0070041 EquivalentTo 'intellectual disability, autosomal dominant 11'
http://purl.obolibrary.org/obo/DOID_0070042
http://purl.obolibrary.org/obo/DOID_0070042 EquivalentTo 'intellectual disability, autosomal dominant 12'
http://purl.obolibrary.org/obo/DOID_0070040
http://purl.obolibrary.org/obo/DOID_0070040 EquivalentTo 'intellectual disability, autosomal dominant 10'
http://purl.obolibrary.org/obo/DOID_0070007
http://purl.obolibrary.org/obo/DOID_0070007 EquivalentTo 'Seckel syndrome 1'
http://purl.obolibrary.org/obo/DOID_0070008
http://purl.obolibrary.org/obo/DOID_0070008 EquivalentTo 'Seckel syndrome 10'
http://purl.obolibrary.org/obo/DOID_0070005
http://purl.obolibrary.org/obo/DOID_0070005 EquivalentTo 'Seckel syndrome 9'
http://purl.obolibrary.org/obo/DOID_0070006
http://purl.obolibrary.org/obo/DOID_0070006 EquivalentTo 'Seckel syndrome 6'
http://purl.obolibrary.org/obo/DOID_0070009
http://purl.obolibrary.org/obo/DOID_0070009 EquivalentTo 'Seckel syndrome 8'
http://purl.obolibrary.org/obo/DOID_0070010
http://purl.obolibrary.org/obo/DOID_0070010 EquivalentTo 'Seckel syndrome 4'
http://purl.obolibrary.org/obo/DOID_0070011
http://purl.obolibrary.org/obo/DOID_0070011 EquivalentTo 'Seckel syndrome 7'
http://purl.obolibrary.org/obo/DOID_0070018
http://purl.obolibrary.org/obo/DOID_0070018 EquivalentTo 'dyskeratosis congenita, autosomal dominant 3'
http://purl.obolibrary.org/obo/DOID_0070019
http://purl.obolibrary.org/obo/DOID_0070019 EquivalentTo 'dyskeratosis congenita, autosomal recessive 3'
http://purl.obolibrary.org/obo/DOID_0070016
http://purl.obolibrary.org/obo/DOID_0070016 EquivalentTo 'dyskeratosis congenita, autosomal dominant 2'
http://purl.obolibrary.org/obo/DOID_0070017
http://purl.obolibrary.org/obo/DOID_0070017 EquivalentTo 'dyskeratosis congenita, autosomal recessive 2'
http://purl.obolibrary.org/obo/DOID_0070014
http://purl.obolibrary.org/obo/DOID_0070014 EquivalentTo 'dyskeratosis congenita, autosomal dominant 1'
http://purl.obolibrary.org/obo/DOID_0070015
http://purl.obolibrary.org/obo/DOID_0070015 EquivalentTo 'dyskeratosis congenita, autosomal recessive 1'
http://purl.obolibrary.org/obo/DOID_0070012
http://purl.obolibrary.org/obo/DOID_0070012 EquivalentTo 'Seckel syndrome 5'
http://purl.obolibrary.org/obo/DOID_0070013
http://purl.obolibrary.org/obo/DOID_0070013 EquivalentTo 'Seckel syndrome 2'
http://purl.obolibrary.org/obo/DOID_0070021
http://purl.obolibrary.org/obo/DOID_0070021 EquivalentTo 'autosomal recessive dyskeratosis congenita 4'
http://purl.obolibrary.org/obo/DOID_0070022
http://purl.obolibrary.org/obo/DOID_0070022 EquivalentTo 'dyskeratosis congenita, autosomal recessive 5'
http://purl.obolibrary.org/obo/DOID_0070020
http://purl.obolibrary.org/obo/DOID_0070020 EquivalentTo 'dyskeratosis congenita, autosomal recessive 5'
http://purl.obolibrary.org/obo/HP_0000074
http://purl.obolibrary.org/obo/NCIT_C2858
'adrenal cortex neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C2858
http://purl.obolibrary.org/obo/OMIMPS_164400
'cerebellar ataxia' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_164400
http://purl.obolibrary.org/obo/SCTID_387922007
'endocrine gland neoplasm' EquivalentTo http://purl.obolibrary.org/obo/SCTID_387922007
http://purl.obolibrary.org/obo/DOID_0070089
http://purl.obolibrary.org/obo/DOID_0070089 EquivalentTo 'SCZD13'
http://purl.obolibrary.org/obo/DOID_0070090
http://purl.obolibrary.org/obo/DOID_0070090 EquivalentTo 'schizophrenia 14'
http://purl.obolibrary.org/obo/DOID_0070091
http://purl.obolibrary.org/obo/DOID_0070091 EquivalentTo 'schizophrenia 15'
http://purl.obolibrary.org/obo/DOID_0070098
http://purl.obolibrary.org/obo/DOID_0070098 EquivalentTo 'oculocutaneous albinism type 4'
http://purl.obolibrary.org/obo/DOID_0070099
http://purl.obolibrary.org/obo/DOID_0070099 EquivalentTo 'oculocutaneous albinism type 5'
http://purl.obolibrary.org/obo/DOID_0070096
http://purl.obolibrary.org/obo/DOID_0070096 EquivalentTo 'oculocutaneous albinism type 2'
http://purl.obolibrary.org/obo/DOID_0070097
http://purl.obolibrary.org/obo/DOID_0070097 EquivalentTo 'oculocutaneous albinism type 3'
http://purl.obolibrary.org/obo/DOID_0070094
http://purl.obolibrary.org/obo/DOID_0070094 EquivalentTo 'oculocutaneous albinism type 1A'
http://purl.obolibrary.org/obo/DOID_0070095
http://purl.obolibrary.org/obo/DOID_0070095 EquivalentTo 'oculocutaneous albinism type 1B'
http://purl.obolibrary.org/obo/DOID_0070092
http://purl.obolibrary.org/obo/DOID_0070092 EquivalentTo 'schizophrenia 16'
http://purl.obolibrary.org/obo/DOID_0070093
http://purl.obolibrary.org/obo/DOID_0070093 EquivalentTo 'schizophrenia 18'
http://purl.obolibrary.org/obo/DOID_0070069
http://purl.obolibrary.org/obo/DOID_0070069 EquivalentTo 'intellectual disability, autosomal dominant 39'
http://purl.obolibrary.org/obo/DOID_0070067
http://purl.obolibrary.org/obo/DOID_0070067 EquivalentTo 'intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome'
http://purl.obolibrary.org/obo/DOID_0070068
http://purl.obolibrary.org/obo/DOID_0070068 EquivalentTo 'intellectual disability, autosomal dominant 38'
http://purl.obolibrary.org/obo/DOID_0070077
http://purl.obolibrary.org/obo/DOID_0070077 EquivalentTo 'SCZD1'
http://purl.obolibrary.org/obo/DOID_0070074
http://purl.obolibrary.org/obo/DOID_0070074 EquivalentTo 'micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome'
http://purl.obolibrary.org/obo/DOID_0070075
http://purl.obolibrary.org/obo/DOID_0070075 EquivalentTo 'Kleefstra syndrome 1'
http://purl.obolibrary.org/obo/DOID_0070072
http://purl.obolibrary.org/obo/DOID_0070072 EquivalentTo 'intellectual disability, autosomal dominant 42'
http://purl.obolibrary.org/obo/DOID_0070073
http://purl.obolibrary.org/obo/DOID_0070073 EquivalentTo 'intellectual disability, autosomal dominant 43'
http://purl.obolibrary.org/obo/DOID_0070070
http://purl.obolibrary.org/obo/DOID_0070070 EquivalentTo 'intellectual disability, autosomal dominant 40'
http://purl.obolibrary.org/obo/DOID_0070071
http://purl.obolibrary.org/obo/DOID_0070071 EquivalentTo 'intellectual disability, autosomal dominant 41; MRD41'
http://purl.obolibrary.org/obo/DOID_0070078
http://purl.obolibrary.org/obo/DOID_0070078 EquivalentTo 'SCZD2'
http://purl.obolibrary.org/obo/DOID_0070079
http://purl.obolibrary.org/obo/DOID_0070079 EquivalentTo 'SCZD3'
http://purl.obolibrary.org/obo/DOID_0070080
http://purl.obolibrary.org/obo/DOID_0070080 EquivalentTo 'schizophrenia 4'
http://purl.obolibrary.org/obo/DOID_0070087
http://purl.obolibrary.org/obo/DOID_0070087 EquivalentTo 'schizophrenia 11'
http://purl.obolibrary.org/obo/DOID_0070088
http://purl.obolibrary.org/obo/DOID_0070088 EquivalentTo 'schizophrenia 12'
http://purl.obolibrary.org/obo/DOID_0070085
http://purl.obolibrary.org/obo/DOID_0070085 EquivalentTo 'schizophrenia 9'
http://purl.obolibrary.org/obo/DOID_0070086
http://purl.obolibrary.org/obo/DOID_0070086 EquivalentTo 'SCZD10'
http://purl.obolibrary.org/obo/DOID_0070083
http://purl.obolibrary.org/obo/DOID_0070083 EquivalentTo 'SCZD7'
http://purl.obolibrary.org/obo/DOID_0070084
http://purl.obolibrary.org/obo/DOID_0070084 EquivalentTo 'SCZD8'
http://purl.obolibrary.org/obo/DOID_0070081
http://purl.obolibrary.org/obo/DOID_0070081 EquivalentTo 'SCZD5'
http://purl.obolibrary.org/obo/DOID_0070082
http://purl.obolibrary.org/obo/DOID_0070082 EquivalentTo 'SCZD6'
http://purl.obolibrary.org/obo/DOID_0070049
http://purl.obolibrary.org/obo/DOID_0070049 EquivalentTo 'severe intellectual disability-progressive spastic diplegia syndrome'
http://purl.obolibrary.org/obo/DOID_0070047
http://purl.obolibrary.org/obo/DOID_0070047 EquivalentTo 'intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome'
http://purl.obolibrary.org/obo/DOID_0070048
http://purl.obolibrary.org/obo/DOID_0070048 EquivalentTo 'severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome'
http://purl.obolibrary.org/obo/DOID_0070045
http://purl.obolibrary.org/obo/DOID_0070045 EquivalentTo 'intellectual disability, autosomal dominant 15'
http://purl.obolibrary.org/obo/DOID_0070046
http://purl.obolibrary.org/obo/DOID_0070046 EquivalentTo 'intellectual disability, autosomal dominant 16'
http://purl.obolibrary.org/obo/DOID_0070054
http://purl.obolibrary.org/obo/DOID_0070054 EquivalentTo 'intellectual disability, autosomal dominant 24'
http://purl.obolibrary.org/obo/DOID_0070055
http://purl.obolibrary.org/obo/DOID_0070055 EquivalentTo 'AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome'
http://purl.obolibrary.org/obo/DOID_0070052
http://purl.obolibrary.org/obo/DOID_0070052 EquivalentTo 'intellectual disability, autosomal dominant 22'
http://purl.obolibrary.org/obo/DOID_0070053
http://purl.obolibrary.org/obo/DOID_0070053 EquivalentTo 'intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency'
http://purl.obolibrary.org/obo/DOID_0070050
http://purl.obolibrary.org/obo/DOID_0070050 EquivalentTo 'intellectual disability, autosomal dominant 20'
http://purl.obolibrary.org/obo/DOID_0070051
http://purl.obolibrary.org/obo/DOID_0070051 EquivalentTo 'intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome'
http://purl.obolibrary.org/obo/DOID_0070058
http://purl.obolibrary.org/obo/DOID_0070058 EquivalentTo 'ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder'
http://purl.obolibrary.org/obo/DOID_0070059
http://purl.obolibrary.org/obo/DOID_0070059 EquivalentTo 'intellectual disability, autosomal dominant 29'
http://purl.obolibrary.org/obo/DOID_0070056
http://purl.obolibrary.org/obo/DOID_0070056 EquivalentTo 'autism spectrum disorder due to AUTS2 deficiency'
http://purl.obolibrary.org/obo/DOID_0070057
http://purl.obolibrary.org/obo/DOID_0070057 EquivalentTo 'intellectual disability, autosomal dominant 27'
http://purl.obolibrary.org/obo/DOID_0070065
http://purl.obolibrary.org/obo/DOID_0070065 EquivalentTo 'intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome'
http://purl.obolibrary.org/obo/DOID_0070066
http://purl.obolibrary.org/obo/DOID_0070066 EquivalentTo 'microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome'
http://purl.obolibrary.org/obo/DOID_0070063
http://purl.obolibrary.org/obo/DOID_0070063 EquivalentTo 'intellectual disability, autosomal dominant 33'
http://purl.obolibrary.org/obo/DOID_0070064
http://purl.obolibrary.org/obo/DOID_0070064 EquivalentTo 'intellectual disability, autosomal dominant 34'
http://purl.obolibrary.org/obo/DOID_0070061
http://purl.obolibrary.org/obo/DOID_0070061 EquivalentTo 'PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation'
http://purl.obolibrary.org/obo/DOID_0070062
http://purl.obolibrary.org/obo/DOID_0070062 EquivalentTo 'autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome'
http://purl.obolibrary.org/obo/DOID_0070060
http://purl.obolibrary.org/obo/DOID_0070060 EquivalentTo 'intellectual disability, autosomal dominant 30'
http://purl.obolibrary.org/obo/DOID_0070148
http://purl.obolibrary.org/obo/DOID_0070148 EquivalentTo 'hereditary sensory and autonomic neuropathy type 1B'
http://purl.obolibrary.org/obo/DOID_0070149
http://purl.obolibrary.org/obo/DOID_0070149 EquivalentTo 'hereditary sensory and autonomic neuropathy type 7'
http://purl.obolibrary.org/obo/DOID_0070146
http://purl.obolibrary.org/obo/DOID_0070146 EquivalentTo 'hereditary sensory and autonomic neuropathy type 4'
http://purl.obolibrary.org/obo/DOID_0070147
http://purl.obolibrary.org/obo/DOID_0070147 EquivalentTo 'neuropathy, hereditary sensory, type 2C'
http://purl.obolibrary.org/obo/DOID_0070144
http://purl.obolibrary.org/obo/DOID_0070144 EquivalentTo 'autosomal recessive cutis laxa type 1'
http://purl.obolibrary.org/obo/DOID_0070145
http://purl.obolibrary.org/obo/DOID_0070145 EquivalentTo 'hereditary sensory and autonomic neuropathy type 5'
http://purl.obolibrary.org/obo/DOID_0070153
http://purl.obolibrary.org/obo/DOID_0070153 EquivalentTo 'congenital insensitivity to pain-hypohidrosis syndrome'
http://purl.obolibrary.org/obo/DOID_0070154
http://purl.obolibrary.org/obo/DOID_0070154 EquivalentTo 'neuropathy, hereditary sensory, type 1F'
http://purl.obolibrary.org/obo/DOID_0070151
http://purl.obolibrary.org/obo/DOID_0070151 EquivalentTo 'hereditary sensory and autonomic neuropathy type 6'
http://purl.obolibrary.org/obo/DOID_0070152
http://purl.obolibrary.org/obo/DOID_0070152 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 1A'
http://purl.obolibrary.org/obo/DOID_0070150
http://purl.obolibrary.org/obo/DOID_0070150 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 2B'
http://purl.obolibrary.org/obo/DOID_0070159
http://purl.obolibrary.org/obo/DOID_0070159 EquivalentTo 'hereditary sensory neuropathy X-linked'
http://purl.obolibrary.org/obo/DOID_0070157
http://purl.obolibrary.org/obo/DOID_0070157 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 1C'
http://purl.obolibrary.org/obo/DOID_0070158
http://purl.obolibrary.org/obo/DOID_0070158 EquivalentTo 'hereditary sensory neuropathy-deafness-dementia syndrome'
http://purl.obolibrary.org/obo/DOID_0070155
http://purl.obolibrary.org/obo/DOID_0070155 EquivalentTo 'neuropathy, hereditary sensory and autonomic, type 2A'
http://purl.obolibrary.org/obo/DOID_0070156
http://purl.obolibrary.org/obo/DOID_0070156 EquivalentTo 'neuropathy, hereditary sensory, type 1D'
http://purl.obolibrary.org/obo/DOID_0070162
http://purl.obolibrary.org/obo/DOID_0070162 EquivalentTo 'hereditary sensory and autonomic neuropathy type 1'
http://purl.obolibrary.org/obo/DOID_0070160
http://purl.obolibrary.org/obo/DOID_0070160 EquivalentTo 'neuropathy, hereditary sensory, atypical'
http://purl.obolibrary.org/obo/DOID_0070161
http://purl.obolibrary.org/obo/DOID_0070161 EquivalentTo 'hereditary sensory and autonomic neuropathy type 2'
http://purl.obolibrary.org/obo/DOID_0070128
http://purl.obolibrary.org/obo/DOID_0070128 EquivalentTo 'congenital nongoitrous hypothryoidism 6'
http://purl.obolibrary.org/obo/DOID_0070129
http://purl.obolibrary.org/obo/DOID_0070129 EquivalentTo 'autosomal recessive cutis laxa type 2d'
http://purl.obolibrary.org/obo/DOID_0070126
http://purl.obolibrary.org/obo/DOID_0070126 EquivalentTo 'hypothyroidism due to TSH receptor mutations'
http://purl.obolibrary.org/obo/DOID_0070127
http://purl.obolibrary.org/obo/DOID_0070127 EquivalentTo 'congenital nongoitrous hypothryoidism 3'
http://purl.obolibrary.org/obo/DOID_0070124
http://purl.obolibrary.org/obo/DOID_0070124 EquivalentTo 'hypothyroidism, congenital, nongoitrous, 2'
http://purl.obolibrary.org/obo/DOID_0070125
http://purl.obolibrary.org/obo/DOID_0070125 EquivalentTo 'hypothyroidism, congenital, Nongoitrous, 5'
http://purl.obolibrary.org/obo/DOID_0070122
http://purl.obolibrary.org/obo/DOID_0070122 EquivalentTo 'Meckel syndrome, type 8'
http://purl.obolibrary.org/obo/DOID_0070123
http://purl.obolibrary.org/obo/DOID_0070123 EquivalentTo 'isolated thyroid-stimulating hormone deficiency'
http://purl.obolibrary.org/obo/DOID_0070131
http://purl.obolibrary.org/obo/DOID_0070131 EquivalentTo 'cutis laxa, autosomal dominant 3'
http://purl.obolibrary.org/obo/DOID_0070132
http://purl.obolibrary.org/obo/DOID_0070132 EquivalentTo 'ALDH18A1-related de Barsy syndrome'
http://purl.obolibrary.org/obo/DOID_0070130
http://purl.obolibrary.org/obo/DOID_0070130 EquivalentTo 'cutis laxa, autosomal dominant 1'
http://purl.obolibrary.org/obo/DOID_0070139
http://purl.obolibrary.org/obo/DOID_0070139 EquivalentTo 'cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies'
http://purl.obolibrary.org/obo/DOID_0070137
http://purl.obolibrary.org/obo/DOID_0070137 EquivalentTo 'autosomal recessive cutis laxa type 2B'
http://purl.obolibrary.org/obo/DOID_0070138
http://purl.obolibrary.org/obo/DOID_0070138 EquivalentTo 'PYCR1-related de Barsy syndrome'
http://purl.obolibrary.org/obo/DOID_0070135
http://purl.obolibrary.org/obo/DOID_0070135 EquivalentTo 'cutis laxa, autosomal recessive, type 1A'
http://purl.obolibrary.org/obo/DOID_0070136
http://purl.obolibrary.org/obo/DOID_0070136 EquivalentTo 'autosomal recessive cutis laxa type 2, classic type'
http://purl.obolibrary.org/obo/DOID_0070133
http://purl.obolibrary.org/obo/DOID_0070133 EquivalentTo 'cutis laxa, autosomal recessive, type 1B'
http://purl.obolibrary.org/obo/DOID_0070134
http://purl.obolibrary.org/obo/DOID_0070134 EquivalentTo 'autosomal recessive cutis laxa type 2A'
http://purl.obolibrary.org/obo/DOID_0070142
http://purl.obolibrary.org/obo/DOID_0070142 EquivalentTo 'autosomal dominant cutis laxa'
http://purl.obolibrary.org/obo/DOID_0070143
http://purl.obolibrary.org/obo/DOID_0070143 EquivalentTo 'de Barsy syndrome'
http://purl.obolibrary.org/obo/DOID_0070140
http://purl.obolibrary.org/obo/DOID_0070140 EquivalentTo 'autosomal recessive cutis laxa type 2c'
http://purl.obolibrary.org/obo/DOID_0070141
http://purl.obolibrary.org/obo/DOID_0070141 EquivalentTo 'autosomal recessive cutis laxa type 2, classic type'
http://purl.obolibrary.org/obo/DOID_0070100
http://purl.obolibrary.org/obo/DOID_0070100 EquivalentTo 'oculocutaneous albinism type 7'
http://purl.obolibrary.org/obo/DOID_0070117
http://purl.obolibrary.org/obo/DOID_0070117 EquivalentTo 'Meckel syndrome, type 3'
http://purl.obolibrary.org/obo/DOID_0070118
http://purl.obolibrary.org/obo/DOID_0070118 EquivalentTo 'Meckel syndrome, type 4'
http://purl.obolibrary.org/obo/DOID_0070115
http://purl.obolibrary.org/obo/DOID_0070115 EquivalentTo 'Meckel syndrome, type 1'
http://purl.obolibrary.org/obo/DOID_0070116
http://purl.obolibrary.org/obo/DOID_0070116 EquivalentTo 'Meckel syndrome, type 2'
http://purl.obolibrary.org/obo/DOID_0070113
http://purl.obolibrary.org/obo/DOID_0070113 EquivalentTo 'Niemann-Pick disease, type C1'
http://purl.obolibrary.org/obo/DOID_0070114
http://purl.obolibrary.org/obo/DOID_0070114 EquivalentTo 'Niemann-Pick disease, type C2'
http://purl.obolibrary.org/obo/DOID_0070111
http://purl.obolibrary.org/obo/DOID_0070111 EquivalentTo 'Niemann-Pick disease type A'
http://purl.obolibrary.org/obo/DOID_0070112
http://purl.obolibrary.org/obo/DOID_0070112 EquivalentTo 'Niemann-Pick disease type B'
http://purl.obolibrary.org/obo/DOID_0070119
http://purl.obolibrary.org/obo/DOID_0070119 EquivalentTo 'Meckel syndrome, type 5'
http://purl.obolibrary.org/obo/DOID_0070120
http://purl.obolibrary.org/obo/DOID_0070120 EquivalentTo 'Meckel syndrome, type 6'
http://purl.obolibrary.org/obo/DOID_0070121
http://purl.obolibrary.org/obo/DOID_0070121 EquivalentTo 'NPHP3-related Meckel-like syndrome'
http://purl.obolibrary.org/obo/OMIM_618013
'deafness, autosomal recessive 109' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618013
http://purl.obolibrary.org/obo/OMIM_618008
'epileptic encephalopathy, early infantile, 65' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618008
http://purl.obolibrary.org/obo/OMIM_618003
'deafness, autosomal recessive 57' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618003
http://purl.obolibrary.org/obo/OMIM_618004
'epileptic encephalopathy, early infantile, 64' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618004
http://purl.obolibrary.org/obo/OMIM_301008
'intellectual disability, X-linked, syndromic, Houge type' EquivalentTo http://purl.obolibrary.org/obo/OMIM_301008
http://purl.obolibrary.org/obo/OMIM_301006
'Galloway-Mowat syndrome 2, X-linked' EquivalentTo http://purl.obolibrary.org/obo/OMIM_301006
http://purl.obolibrary.org/obo/NCBITaxon_52283
http://purl.obolibrary.org/obo/GARD_0012784
http://purl.obolibrary.org/obo/GARD_0012784 EquivalentTo 'livedoid vasculopathy'
http://purl.obolibrary.org/obo/NCIT_C40039
'benign ovarian mucinous tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C40039
http://purl.obolibrary.org/obo/NCIT_C126357
'peritoneal solitary fibrous tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C126357
http://purl.obolibrary.org/obo/HP_0009064
http://purl.obolibrary.org/obo/DOID_0080293
http://purl.obolibrary.org/obo/DOID_0080293 EquivalentTo 'short-rib thoracic dysplasia 18 with polydactyly'
http://purl.obolibrary.org/obo/DOID_0080294
http://purl.obolibrary.org/obo/DOID_0080294 EquivalentTo 'charcot-marie-tooth disease, dominant intermediate G'
http://purl.obolibrary.org/obo/DOID_0080295
http://purl.obolibrary.org/obo/DOID_0080295 EquivalentTo 'short-rib thoracic dysplasia 19 with or without polydactyly'
http://purl.obolibrary.org/obo/DOID_0080296
http://purl.obolibrary.org/obo/DOID_0080296 EquivalentTo 'leukodystrophy, hypomyelinating, 14'
http://purl.obolibrary.org/obo/DOID_0080290
http://purl.obolibrary.org/obo/DOID_0080290 EquivalentTo 'erythrocytosis, familial, 5'
http://purl.obolibrary.org/obo/DOID_0080291
http://purl.obolibrary.org/obo/DOID_0080291 EquivalentTo 'epileptic encephalopathy, early infantile, 59'
http://purl.obolibrary.org/obo/DOID_0080292
http://purl.obolibrary.org/obo/DOID_0080292 EquivalentTo 'retinitis pigmentosa 81'
http://purl.obolibrary.org/obo/DOID_0080286
http://purl.obolibrary.org/obo/DOID_0080286 EquivalentTo 'spinocerebellar ataxia 44'
http://purl.obolibrary.org/obo/DOID_0080287
http://purl.obolibrary.org/obo/DOID_0080287 EquivalentTo 'spinocerebellar ataxia 45'
http://purl.obolibrary.org/obo/DOID_0080288
http://purl.obolibrary.org/obo/DOID_0080288 EquivalentTo 'spinocerebellar ataxia 46'
http://purl.obolibrary.org/obo/DOID_0080289
http://purl.obolibrary.org/obo/DOID_0080289 EquivalentTo 'orofaciodigital syndrome 17'
http://purl.obolibrary.org/obo/DOID_0080297
http://purl.obolibrary.org/obo/DOID_0080297 EquivalentTo 'coffin-siris syndrome 6'
http://purl.obolibrary.org/obo/DOID_0080298
http://purl.obolibrary.org/obo/DOID_0080298 EquivalentTo 'generalized lipodystrophy'
http://purl.obolibrary.org/obo/DOID_0080299
http://purl.obolibrary.org/obo/DOID_0080299 EquivalentTo 'partial lipodystrophy'
http://purl.obolibrary.org/obo/DOID_0080271
http://purl.obolibrary.org/obo/DOID_0080271 EquivalentTo 'nephrotic syndrome 15'
http://purl.obolibrary.org/obo/DOID_0080272
http://purl.obolibrary.org/obo/DOID_0080272 EquivalentTo 'nephrotic syndrome 16'
http://purl.obolibrary.org/obo/DOID_0080273
http://purl.obolibrary.org/obo/DOID_0080273 EquivalentTo 'polycystic kidney disease 5'
http://purl.obolibrary.org/obo/DOID_0080274
http://purl.obolibrary.org/obo/DOID_0080274 EquivalentTo 'multiple mitochondrial dysfunctions syndrome 5'
http://purl.obolibrary.org/obo/DOID_0080270
http://purl.obolibrary.org/obo/DOID_0080270 EquivalentTo 'deafness, autosomal dominant 34, with or without inflammation'
http://purl.obolibrary.org/obo/DOID_0080268
http://purl.obolibrary.org/obo/DOID_0080268 EquivalentTo 'deafness, autosomal dominant 72'
http://purl.obolibrary.org/obo/DOID_0080269
http://purl.obolibrary.org/obo/DOID_0080269 EquivalentTo 'deafness, autosomal dominant 73'
http://purl.obolibrary.org/obo/DOID_0080264
http://purl.obolibrary.org/obo/DOID_0080264 EquivalentTo 'exudative vitreoretinopathy 7'
http://purl.obolibrary.org/obo/DOID_0080265
http://purl.obolibrary.org/obo/DOID_0080265 EquivalentTo 'nephrotic syndrome 14'
http://purl.obolibrary.org/obo/DOID_0080266
http://purl.obolibrary.org/obo/DOID_0080266 EquivalentTo 'ciliary dyskinesia, primary, 37'
http://purl.obolibrary.org/obo/DOID_0080267
http://purl.obolibrary.org/obo/DOID_0080267 EquivalentTo 'deafness, autosomal dominant 71'
http://purl.obolibrary.org/obo/DOID_0080282
http://purl.obolibrary.org/obo/DOID_0080282 EquivalentTo 'epileptic encephalopathy, early infantile, 56'
http://purl.obolibrary.org/obo/DOID_0080283
http://purl.obolibrary.org/obo/DOID_0080283 EquivalentTo 'epileptic encephalopathy, early infantile, 55'
http://purl.obolibrary.org/obo/DOID_0080284
http://purl.obolibrary.org/obo/DOID_0080284 EquivalentTo 'epileptic encephalopathy, early infantile, 57'
http://purl.obolibrary.org/obo/DOID_0080285
http://purl.obolibrary.org/obo/DOID_0080285 EquivalentTo 'epileptic encephalopathy, early infantile, 58'
http://purl.obolibrary.org/obo/DOID_0080280
http://purl.obolibrary.org/obo/DOID_0080280 EquivalentTo 'fibromatosis, gingival, 5'
http://purl.obolibrary.org/obo/DOID_0080281
http://purl.obolibrary.org/obo/DOID_0080281 EquivalentTo 'schizophrenia 19'
http://purl.obolibrary.org/obo/DOID_0080279
http://purl.obolibrary.org/obo/DOID_0080279 EquivalentTo 'joubert syndrome 33'
http://purl.obolibrary.org/obo/DOID_0080275
http://purl.obolibrary.org/obo/DOID_0080275 EquivalentTo 'joubert syndrome 30'
http://purl.obolibrary.org/obo/DOID_0080277
http://purl.obolibrary.org/obo/DOID_0080277 EquivalentTo 'joubert syndrome 31'
http://purl.obolibrary.org/obo/DOID_0080278
http://purl.obolibrary.org/obo/DOID_0080278 EquivalentTo 'joubert syndrome 32'
http://purl.obolibrary.org/obo/DOID_0080250
http://purl.obolibrary.org/obo/DOID_0080250 EquivalentTo 'erythrokeratodermia variabilis et progressiva 4'
http://purl.obolibrary.org/obo/DOID_0080251
http://purl.obolibrary.org/obo/DOID_0080251 EquivalentTo 'erythrokeratodermia variabilis et progressiva 5'
http://purl.obolibrary.org/obo/DOID_0080252
http://purl.obolibrary.org/obo/DOID_0080252 EquivalentTo 'spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy'
http://purl.obolibrary.org/obo/DOID_0080246
http://purl.obolibrary.org/obo/DOID_0080246 EquivalentTo 'Galloway-Mowat syndrome 4'
http://purl.obolibrary.org/obo/DOID_0080247
http://purl.obolibrary.org/obo/DOID_0080247 EquivalentTo 'Galloway-Mowat syndrome 5'
http://purl.obolibrary.org/obo/DOID_0080248
http://purl.obolibrary.org/obo/DOID_0080248 EquivalentTo 'erythrokeratodermia variabilis et progressiva 2'
http://purl.obolibrary.org/obo/DOID_0080249
http://purl.obolibrary.org/obo/DOID_0080249 EquivalentTo 'erythrokeratodermia variabilis et progressiva 3'
http://purl.obolibrary.org/obo/DOID_0080242
http://purl.obolibrary.org/obo/DOID_0080242 EquivalentTo 'intellectual disability, X-linked, syndromic, Houge type'
http://purl.obolibrary.org/obo/DOID_0080243
http://purl.obolibrary.org/obo/DOID_0080243 EquivalentTo 'amelogenesis imperfecta type 3B'
http://purl.obolibrary.org/obo/DOID_0080244
http://purl.obolibrary.org/obo/DOID_0080244 EquivalentTo 'Galloway-Mowat syndrome 2, X-linked'
http://purl.obolibrary.org/obo/DOID_0080245
http://purl.obolibrary.org/obo/DOID_0080245 EquivalentTo 'Galloway-Mowat syndrome 3'
http://purl.obolibrary.org/obo/DOID_0080260
http://purl.obolibrary.org/obo/DOID_0080260 EquivalentTo 'spinocerebellar ataxia, autosomal recessive 26'
http://purl.obolibrary.org/obo/DOID_0080261
http://purl.obolibrary.org/obo/DOID_0080261 EquivalentTo 'deafness, autosomal recessive 106'
http://purl.obolibrary.org/obo/DOID_0080262
http://purl.obolibrary.org/obo/DOID_0080262 EquivalentTo 'deafness, autosomal recessive 107'
http://purl.obolibrary.org/obo/DOID_0080263
http://purl.obolibrary.org/obo/DOID_0080263 EquivalentTo 'deafness, autosomal recessive 108'
http://purl.obolibrary.org/obo/DOID_0080257
http://purl.obolibrary.org/obo/DOID_0080257 EquivalentTo 'ichthyosis, congenital, autosomal recessive 13'
http://purl.obolibrary.org/obo/DOID_0080258
http://purl.obolibrary.org/obo/DOID_0080258 EquivalentTo 'ichthyosis, congenital, autosomal recessive 14'
http://purl.obolibrary.org/obo/DOID_0080259
http://purl.obolibrary.org/obo/DOID_0080259 EquivalentTo 'spinocerebellar ataxia, autosomal recessive 25'
http://purl.obolibrary.org/obo/DOID_0080253
http://purl.obolibrary.org/obo/DOID_0080253 EquivalentTo 'Meckel syndrome 13'
http://purl.obolibrary.org/obo/DOID_0080254
http://purl.obolibrary.org/obo/DOID_0080254 EquivalentTo 'orofaciodigital syndrome 16'
http://purl.obolibrary.org/obo/DOID_0080255
http://purl.obolibrary.org/obo/DOID_0080255 EquivalentTo 'Meier-Gorlin syndrome 8'
http://purl.obolibrary.org/obo/DOID_0080256
http://purl.obolibrary.org/obo/DOID_0080256 EquivalentTo 'Perrault syndrome 6'
http://purl.obolibrary.org/obo/DOID_0080230
http://purl.obolibrary.org/obo/DOID_0080230 EquivalentTo 'intellectual disability, autosomal dominant 54'
http://purl.obolibrary.org/obo/DOID_0080224
http://purl.obolibrary.org/obo/DOID_0080224 EquivalentTo 'generalized dominant dystrophic epidermolysis bullosa'
http://purl.obolibrary.org/obo/DOID_0080225
http://purl.obolibrary.org/obo/DOID_0080225 EquivalentTo 'amyotrophic lateral sclerosis type 23'
http://purl.obolibrary.org/obo/DOID_0080226
http://purl.obolibrary.org/obo/DOID_0080226 EquivalentTo 'intellectual disability, autosomal dominant 56'
http://purl.obolibrary.org/obo/DOID_0080227
http://purl.obolibrary.org/obo/DOID_0080227 EquivalentTo 'intellectual disability, autosomal dominant 55, with seizures'
http://purl.obolibrary.org/obo/DOID_0080220
http://purl.obolibrary.org/obo/DOID_0080220 EquivalentTo 'MAFD1'
http://purl.obolibrary.org/obo/DOID_0080221
http://purl.obolibrary.org/obo/DOID_0080221 EquivalentTo 'MAFD2'
http://purl.obolibrary.org/obo/DOID_0080222
http://purl.obolibrary.org/obo/DOID_0080222 EquivalentTo 'pseudohypoparathyroidism type 1B'
http://purl.obolibrary.org/obo/DOID_0080223
http://purl.obolibrary.org/obo/DOID_0080223 EquivalentTo 'epidermolytic palmoplantar keratoderma'
http://purl.obolibrary.org/obo/DOID_0080228
http://purl.obolibrary.org/obo/DOID_0080228 EquivalentTo 'intellectual disability, autosomal dominant 53'
http://purl.obolibrary.org/obo/DOID_0080240
http://purl.obolibrary.org/obo/DOID_0080240 EquivalentTo 'intellectual disability, X-linked 106'
http://purl.obolibrary.org/obo/DOID_0080241
http://purl.obolibrary.org/obo/DOID_0080241 EquivalentTo 'intellectual disability, X-linked, syndromic, 35'
http://purl.obolibrary.org/obo/DOID_0080235
http://purl.obolibrary.org/obo/DOID_0080235 EquivalentTo 'intellectual disability, autosomal dominant 48'
http://purl.obolibrary.org/obo/DOID_0080236
http://purl.obolibrary.org/obo/DOID_0080236 EquivalentTo 'intellectual disability, autosomal dominant 45'
http://purl.obolibrary.org/obo/DOID_0080237
http://purl.obolibrary.org/obo/DOID_0080237 EquivalentTo 'intellectual disability, autosomal dominant 46'
http://purl.obolibrary.org/obo/DOID_0080238
http://purl.obolibrary.org/obo/DOID_0080238 EquivalentTo 'intellectual disability, autosomal dominant 47'
http://purl.obolibrary.org/obo/DOID_0080231
http://purl.obolibrary.org/obo/DOID_0080231 EquivalentTo 'intellectual disability, autosomal dominant 52'
http://purl.obolibrary.org/obo/DOID_0080232
http://purl.obolibrary.org/obo/DOID_0080232 EquivalentTo 'intellectual disability, autosomal dominant 51'
http://purl.obolibrary.org/obo/DOID_0080233
http://purl.obolibrary.org/obo/DOID_0080233 EquivalentTo 'intellectual disability, autosomal dominant 50'
http://purl.obolibrary.org/obo/DOID_0080234
http://purl.obolibrary.org/obo/DOID_0080234 EquivalentTo 'intellectual disability, autosomal dominant 49'
http://purl.obolibrary.org/obo/DOID_0080239
http://purl.obolibrary.org/obo/DOID_0080239 EquivalentTo 'intellectual disability, autosomal recessive 61'
http://purl.obolibrary.org/obo/DOID_0080202
http://purl.obolibrary.org/obo/DOID_0080202 EquivalentTo 'adenoid cystic carcinoma'
http://purl.obolibrary.org/obo/DOID_0080204
http://purl.obolibrary.org/obo/DOID_0080204 EquivalentTo 'renal hypoplasia (disease)'
http://purl.obolibrary.org/obo/DOID_0080205
http://purl.obolibrary.org/obo/DOID_0080205 EquivalentTo 'congenital anomaly of kidney and urinary tract'
http://purl.obolibrary.org/obo/DOID_0080206
http://purl.obolibrary.org/obo/DOID_0080206 EquivalentTo 'congenital anomalies of kidney and urinary tract 1, susceptibility to'
http://purl.obolibrary.org/obo/DOID_0080207
http://purl.obolibrary.org/obo/DOID_0080207 EquivalentTo 'congenital anomalies of kidney and urinary tract type 2'
http://purl.obolibrary.org/obo/DOID_0080208
http://purl.obolibrary.org/obo/DOID_0080208 EquivalentTo 'non-alcoholic fatty liver disease'
http://purl.obolibrary.org/obo/DOID_0080209
http://purl.obolibrary.org/obo/DOID_0080209 EquivalentTo 'congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome'
http://purl.obolibrary.org/obo/DOID_0080213
http://purl.obolibrary.org/obo/DOID_0080213 EquivalentTo 'punctate palmoplantar keratoderma type 2'
http://purl.obolibrary.org/obo/DOID_0080214
http://purl.obolibrary.org/obo/DOID_0080214 EquivalentTo 'palmoplantar keratoderma, punctate type 1A'
http://purl.obolibrary.org/obo/DOID_0080215
http://purl.obolibrary.org/obo/DOID_0080215 EquivalentTo 'hyperekplexia-epilepsy syndrome'
http://purl.obolibrary.org/obo/DOID_0080216
http://purl.obolibrary.org/obo/DOID_0080216 EquivalentTo 'duodenal atresia (disease)'
http://purl.obolibrary.org/obo/DOID_0080210
http://purl.obolibrary.org/obo/DOID_0080210 EquivalentTo 'primary mediastinal large B-cell lymphoma'
http://purl.obolibrary.org/obo/DOID_0080211
http://purl.obolibrary.org/obo/DOID_0080211 EquivalentTo 'nodal marginal zone B-cell lymphoma'
http://purl.obolibrary.org/obo/DOID_0080212
http://purl.obolibrary.org/obo/DOID_0080212 EquivalentTo 'polycystic kidney disease 4 with or without polycystic liver disease'
http://purl.obolibrary.org/obo/DOID_0080217
http://purl.obolibrary.org/obo/DOID_0080217 EquivalentTo 'lysosomal acid lipase deficiency'
http://purl.obolibrary.org/obo/DOID_0080218
http://purl.obolibrary.org/obo/DOID_0080218 EquivalentTo 'familial spontaneous pneumothorax'
http://purl.obolibrary.org/obo/DOID_0080219
http://purl.obolibrary.org/obo/DOID_0080219 EquivalentTo 'hyperthyroxinemia, dystransthyretinemic'
http://purl.obolibrary.org/obo/NCIT_C2880
'ovarian sertoli-leydig cell tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C2880
http://purl.obolibrary.org/obo/MONDO_0031014
autoimmune gastritis
'autoimmune gastritis' EquivalentTo 'gastritis (disease)' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/DOID_0040090 EquivalentTo 'autoimmune gastritis'
'autoimmune gastritis' SubClassOf 'autoimmune disease of gastrointestinal tract'
'autoimmune gastritis' SubClassOf 'gastritis (disease)'
http://purl.obolibrary.org/obo/MONDO_0031012
autoimmune uveitis
'autoimmune uveitis' EquivalentTo 'uveitis (disease)' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune uveitis' SubClassOf 'autoimmune disease of the nervous system'
http://purl.obolibrary.org/obo/DOID_0040088 EquivalentTo 'autoimmune uveitis'
'autoimmune uveitis' SubClassOf 'autoimmune disease of ear, nose and throat'
'autoimmune uveitis' SubClassOf 'uveitis (disease)'
http://purl.obolibrary.org/obo/MONDO_0031013
autoimmune optic neuritis
'autoimmune optic neuritis' SubClassOf 'autoimmune disease of peripheral nervous system'
http://purl.obolibrary.org/obo/DOID_0040089 EquivalentTo 'autoimmune optic neuritis'
'autoimmune optic neuritis' SubClassOf 'autoimmune disease of central nervous system'
'autoimmune optic neuritis' EquivalentTo 'optic neuritis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune optic neuritis' SubClassOf 'optic neuritis'
http://purl.obolibrary.org/obo/UBERON_0006075
http://purl.obolibrary.org/obo/DOID_0080301
http://purl.obolibrary.org/obo/DOID_0080301 EquivalentTo 'atypical hemolytic-uremic syndrome'
http://purl.obolibrary.org/obo/DOID_0080302
http://purl.obolibrary.org/obo/DOID_0080302 EquivalentTo 'complex sleep apnea'
http://purl.obolibrary.org/obo/DOID_0080303
http://purl.obolibrary.org/obo/DOID_0080303 EquivalentTo 'lung colloid adenocarcinoma'
http://purl.obolibrary.org/obo/DOID_0080304
http://purl.obolibrary.org/obo/DOID_0080304 EquivalentTo 'lung colloid adenocarcinoma'
http://purl.obolibrary.org/obo/DOID_0080300
http://purl.obolibrary.org/obo/DOID_0080300 EquivalentTo 'acquired generalized lipodystrophy'
http://purl.obolibrary.org/obo/DOID_0080309
http://purl.obolibrary.org/obo/DOID_0080309 EquivalentTo 'fatal infantile hypertonic myofibrillar myopathy'
http://purl.obolibrary.org/obo/DOID_0080305
http://purl.obolibrary.org/obo/DOID_0080305 EquivalentTo 'lung signet ring cell carcinoma'
http://purl.obolibrary.org/obo/DOID_0080307
http://purl.obolibrary.org/obo/DOID_0080307 EquivalentTo 'myofibrillar myopathy (disease)'
http://purl.obolibrary.org/obo/DOID_0080308
http://purl.obolibrary.org/obo/DOID_0080308 EquivalentTo 'myofibrillar myopathy 8'
http://purl.obolibrary.org/obo/MESH_D009373
http://purl.obolibrary.org/obo/MESH_D009373 EquivalentTo 'germ cell and embryonal cancer'
http://purl.obolibrary.org/obo/HP_0000979
http://purl.obolibrary.org/obo/CHEBI_15365
http://purl.obolibrary.org/obo/GO_0004339
http://purl.obolibrary.org/obo/NCIT_C7074
'serous neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C7074
http://purl.obolibrary.org/obo/MONDO_0100030
adolescent/adult-onset epilepsy syndrome
'adolescent/adult-onset epilepsy syndrome' SubClassOf 'epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100031
autosomal dominant epilepsy with auditory features
'autosomal dominant epilepsy with auditory features' SubClassOf 'adolescent/adult-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100032
familial temporal lobe epilepsy syndrome
'familial temporal lobe epilepsy syndrome' SubClassOf 'adolescent/adult-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100033
metabolic epilepsy
'metabolic epilepsy' SubClassOf 'epilepsy'
http://purl.obolibrary.org/obo/MONDO_0100034
cerebral folate deficiency
'cerebral folate deficiency' SubClassOf 'rare genetic epilepsy'
'cerebral folate deficiency' SubClassOf 'inborn vitamin metabolic disorder'
'cerebral folate deficiency' SubClassOf 'metabolic epilepsy'
http://purl.obolibrary.org/obo/MONDO_0100035
structural epilepsy
'structural epilepsy' SubClassOf 'epilepsy'
http://purl.obolibrary.org/obo/MONDO_0100036
variable age onset epilepsy
'variable age onset epilepsy' SubClassOf 'epilepsy'
http://purl.obolibrary.org/obo/MONDO_0100020
atypical childhood epilepsy with centrotemporal spikes
'atypical childhood epilepsy with centrotemporal spikes' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100021
photosensitive occipital lobe epilepsy
'photosensitive occipital lobe epilepsy' SubClassOf 'childhood-onset epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100022
neonatal/infantile epilepsy syndrome
'neonatal/infantile epilepsy syndrome' SubClassOf 'epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100023
self-limited familial and non-familial neonatal seizures
'self-limited familial and non-familial neonatal seizures' SubClassOf 'neonatal/infantile epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100024
self-limited familial and non-familial infantile seizures
'self-limited familial and non-familial infantile seizures' SubClassOf 'neonatal/infantile epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100025
epilepsy of infancy with migrating focal seizures
'epilepsy of infancy with migrating focal seizures' SubClassOf 'neonatal/infantile epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100026
myoclonic encephalopathy in non-progressive disorder
'myoclonic encephalopathy in non-progressive disorder' SubClassOf 'neonatal/infantile epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100027
febrile seizures plus, genetic epilepsy with febrile seizures plus
'febrile seizures plus, genetic epilepsy with febrile seizures plus' SubClassOf 'neonatal/infantile epilepsy syndrome'
http://purl.obolibrary.org/obo/MONDO_0100028
immune epilepsy
'immune epilepsy' SubClassOf 'epilepsy'
http://purl.obolibrary.org/obo/MONDO_0100029
antibody mediated epilepsy
'antibody mediated epilepsy' SubClassOf 'immune epilepsy'
http://purl.obolibrary.org/obo/MONDO_0100008
food protein-induced enterocolitis syndrome
'food protein-induced enterocolitis syndrome' SubClassOf 'enterocolitis (disease)'
http://purl.obolibrary.org/obo/MONDO_0036591
adrenal cortex neoplasm
'adrenal cortex neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C2858
'adrenal cortex neoplasm' SubClassOf 'adrenal cortex disease'
'adrenal cortex neoplasm' SubClassOf 'adrenal gland neoplasm'
'adrenal cortex neoplasm' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001235)
http://purl.obolibrary.org/obo/MONDO_0036595
ovarian sertoli-leydig cell tumor
'ovarian sertoli-leydig cell tumor' SubClassOf 'ovarian sex cord-stromal tumor'
'ovarian sertoli-leydig cell tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C2880
http://purl.obolibrary.org/obo/SCTID_238762002
'livedoid vasculopathy' EquivalentTo http://purl.obolibrary.org/obo/SCTID_238762002
http://purl.obolibrary.org/obo/MONDO_0036696
spleen neoplasm
'spleen neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3383
'spleen neoplasm' SubClassOf 'hematopoietic and lymphoid system neoplasm'
'spleen neoplasm' SubClassOf 'splenic disease'
'spleen neoplasm' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002106)
'spleen neoplasm' SubClassOf 'digestive system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0036688
rhabdomyoma
'rhabdomyoma' SubClassOf 'benign muscle neoplasm'
'rhabdomyoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3358
http://purl.obolibrary.org/obo/MONDO_0036491
rare childhood malignant neoplasm
'rare childhood malignant neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C114451
'rare childhood malignant neoplasm' SubClassOf 'rare tumor'
'rare childhood malignant neoplasm' EquivalentTo 'childhood malignant neoplasm' and ('has modifier' some 'rare')
'rare childhood malignant neoplasm' SubClassOf 'childhood malignant neoplasm'
http://purl.obolibrary.org/obo/MONDO_0036482
retinitis pigmentosa 81
'retinitis pigmentosa 81' SubClassOf 'retinitis pigmentosa'
'retinitis pigmentosa 81' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617871
http://purl.obolibrary.org/obo/DOID_0080292 EquivalentTo 'retinitis pigmentosa 81'
http://purl.obolibrary.org/obo/MONDO_0036483
short-rib thoracic dysplasia 18 with polydactyly
http://purl.obolibrary.org/obo/DOID_0080293 EquivalentTo 'short-rib thoracic dysplasia 18 with polydactyly'
'short-rib thoracic dysplasia 18 with polydactyly' SubClassOf 'Jeune syndrome'
'short-rib thoracic dysplasia 18 with polydactyly' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617866
http://purl.obolibrary.org/obo/MONDO_0036484
charcot-marie-tooth disease, dominant intermediate G
http://purl.obolibrary.org/obo/DOID_0080294 EquivalentTo 'charcot-marie-tooth disease, dominant intermediate G'
'charcot-marie-tooth disease, dominant intermediate G' SubClassOf 'intermediate Charcot-Marie-tooth disease'
'charcot-marie-tooth disease, dominant intermediate G' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617882
http://purl.obolibrary.org/obo/NCBITaxon_43075
http://purl.obolibrary.org/obo/MONDO_0036511
childhood malignant kidney neoplasm
'childhood malignant kidney neoplasm' SubClassOf 'kidney cancer'
'childhood malignant kidney neoplasm' EquivalentTo 'kidney cancer' and ('has modifier' some http://purl.obolibrary.org/obo/HP_0011463)
'childhood malignant kidney neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C123907
'childhood malignant kidney neoplasm' SubClassOf 'childhood malignant neoplasm'
'childhood malignant kidney neoplasm' SubClassOf 'childhood kidney neoplasm'
http://purl.obolibrary.org/obo/MONDO_0036501
refractory malignant neoplasm
'refractory malignant neoplasm' SubClassOf 'cancer'
'refractory malignant neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C120186
'refractory malignant neoplasm' EquivalentTo 'cancer' and ('has modifier' some 'refractory')
'refractory malignant neoplasm' SubClassOf 'has modifier' some 'refractory'
http://purl.obolibrary.org/obo/SCTID_448148000
'functioning pituitary gland neoplasm' EquivalentTo http://purl.obolibrary.org/obo/SCTID_448148000
http://purl.obolibrary.org/obo/NCIT_C3114
'hypersensitivity reaction disease' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3114
http://purl.obolibrary.org/obo/NCIT_C3115
'type IV hypersensitivity disease' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3115
http://purl.obolibrary.org/obo/NCIT_C3139
'infratentorial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3139
http://purl.obolibrary.org/obo/SCTID_404808000
'isocyanate induced asthma' EquivalentTo http://purl.obolibrary.org/obo/SCTID_404808000
http://purl.obolibrary.org/obo/MONDO_0036915
benign ovarian mucinous tumor
'benign ovarian mucinous tumor' SubClassOf 'ovarian mucinous neoplasm'
'benign ovarian mucinous tumor' SubClassOf 'benign epithelial neoplasm'
'benign ovarian mucinous tumor' EquivalentTo 'ovarian mucinous neoplasm' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002096)
'benign ovarian mucinous tumor' SubClassOf 'ovarian benign neoplasm'
'benign ovarian mucinous tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C40039
http://purl.obolibrary.org/obo/MONDO_0036976
benign epithelial neoplasm
'benign epithelial neoplasm' EquivalentTo 'epithelial neoplasm' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002096)
'benign epithelial neoplasm' SubClassOf 'benign neoplasm'
'benign epithelial neoplasm' SubClassOf 'epithelial neoplasm'
'benign epithelial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4092
http://purl.obolibrary.org/obo/MONDO_0036990
benign leydig cell tumor
'benign leydig cell tumor' EquivalentTo 'leydig cell tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002096)
'benign leydig cell tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4212
'benign leydig cell tumor' SubClassOf 'leydig cell tumor'
'benign leydig cell tumor' SubClassOf 'benign reproductive system neoplasm'
http://purl.obolibrary.org/obo/NCIT_C3405
'thecoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3405
http://purl.obolibrary.org/obo/MONDO_0036870
lymphatic vessel neoplasm
'lymphatic vessel neoplasm' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0001473
'lymphatic vessel neoplasm' SubClassOf 'vascular disease'
'lymphatic vessel neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3723
'lymphatic vessel neoplasm' SubClassOf 'vascular neoplasm'
'lymphatic vessel neoplasm' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001473)
'lymphatic vessel neoplasm' SubClassOf 'lymphatic system disease'
http://purl.obolibrary.org/obo/NCIT_C3358
'rhabdomyoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3358
http://purl.obolibrary.org/obo/NCIT_C3383
'spleen neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3383
http://purl.obolibrary.org/obo/MONDO_0036779
axillary neoplasm
'axillary neoplasm' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0009472
'axillary neoplasm' SubClassOf 'neoplasm of thorax'
'axillary neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35749
'axillary neoplasm' EquivalentTo 'neoplasm (disease)' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0009472)
http://purl.obolibrary.org/obo/MONDO_0036781
benign axillary neoplasm
'benign axillary neoplasm' SubClassOf 'thoracic benign neoplasm'
'benign axillary neoplasm' EquivalentTo 'axillary neoplasm' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002096)
'benign axillary neoplasm' SubClassOf 'axillary neoplasm'
'benign axillary neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35750
http://linkedlifedata.com/resource/umls/id/C1527304
http://linkedlifedata.com/resource/umls/id/C1527304 EquivalentTo 'allergic disease'
http://purl.obolibrary.org/obo/OBI_1110054
'autoimmune disease' EquivalentTo http://purl.obolibrary.org/obo/OBI_1110054
http://purl.obolibrary.org/obo/HP_0025234
http://purl.obolibrary.org/obo/UBERON_0001898
http://purl.obolibrary.org/obo/NCIT_C3723
'lymphatic vessel neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3723
http://purl.obolibrary.org/obo/SCTID_64479007
'Klebsiella pneumonia' EquivalentTo http://purl.obolibrary.org/obo/SCTID_64479007
http://purl.obolibrary.org/obo/UBERON_0011859
http://purl.obolibrary.org/obo/DOID_7571
http://purl.obolibrary.org/obo/DOID_7571 EquivalentTo 'cystic partially differentiated nephroblastoma'
http://purl.obolibrary.org/obo/SCTID_81598001
'trichomonal vulvovaginitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_81598001
http://purl.obolibrary.org/obo/MONDO_0037003
malignant phyllodes tumor
'malignant phyllodes tumor' SubClassOf 'phyllodes tumor'
'malignant phyllodes tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4275
'malignant phyllodes tumor' SubClassOf 'malignant mixed neoplasm'
'malignant phyllodes tumor' EquivalentTo 'phyllodes tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
http://purl.obolibrary.org/obo/MONDO_0037002
benign phyllodes tumor
'benign phyllodes tumor' SubClassOf 'benign neoplasm'
'benign phyllodes tumor' SubClassOf 'phyllodes tumor'
'benign phyllodes tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4274
'benign phyllodes tumor' EquivalentTo 'phyllodes tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002096)
http://purl.obolibrary.org/obo/MONDO_0027676
congenital anomalies of kidney and urinary tract type 2
'congenital anomalies of kidney and urinary tract type 2' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000074
http://purl.obolibrary.org/obo/DOID_0080207 EquivalentTo 'congenital anomalies of kidney and urinary tract type 2'
'congenital anomalies of kidney and urinary tract type 2' EquivalentTo http://purl.obolibrary.org/obo/OMIM_143400
'congenital anomalies of kidney and urinary tract type 2' SubClassOf 'congenital anomaly of kidney and urinary tract'
http://purl.obolibrary.org/obo/MONDO_0027694
amyotrophic lateral sclerosis type 23
'amyotrophic lateral sclerosis type 23' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617839
http://purl.obolibrary.org/obo/DOID_0080225 EquivalentTo 'amyotrophic lateral sclerosis type 23'
'amyotrophic lateral sclerosis type 23' SubClassOf 'amyotrophic lateral sclerosis'
http://purl.obolibrary.org/obo/FOODON_00001771
http://purl.obolibrary.org/obo/MONDO_0027407
Kleefstra syndrome 1
http://purl.obolibrary.org/obo/DOID_0070075 EquivalentTo 'Kleefstra syndrome 1'
'Kleefstra syndrome 1' SubClassOf 'Kleefstra syndrome'
'Kleefstra syndrome 1' EquivalentTo http://purl.obolibrary.org/obo/OMIM_610253
http://purl.obolibrary.org/obo/MONDO_0027462
autosomal recessive cutis laxa type 2c
http://purl.obolibrary.org/obo/DOID_0070140 EquivalentTo 'autosomal recessive cutis laxa type 2c'
'autosomal recessive cutis laxa type 2c' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617402
'autosomal recessive cutis laxa type 2c' SubClassOf 'autosomal recessive cutis laxa type 2, classic type'
http://purl.obolibrary.org/obo/MONDO_0027451
autosomal recessive cutis laxa type 2d
'autosomal recessive cutis laxa type 2d' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617403
'autosomal recessive cutis laxa type 2d' SubClassOf 'autosomal recessive cutis laxa type 2, classic type'
http://purl.obolibrary.org/obo/DOID_0070129 EquivalentTo 'autosomal recessive cutis laxa type 2d'
http://purl.obolibrary.org/obo/MONDO_0027353
autosomal recessive dyskeratosis congenita 4
http://purl.obolibrary.org/obo/DOID_0070021 EquivalentTo 'autosomal recessive dyskeratosis congenita 4'
'autosomal recessive dyskeratosis congenita 4' SubClassOf 'disease shares features of' some 'dyskeratosis congenita, autosomal dominant 2'
'autosomal recessive dyskeratosis congenita 4' SubClassOf 'dyskeratosis congenita'
http://purl.obolibrary.org/obo/CL_0002258
http://purl.obolibrary.org/obo/NCIT_C8409
'sebaceous gland cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C8409
http://purl.obolibrary.org/obo/NCIT_C8431
'ovarian serous tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C8431
http://purl.obolibrary.org/obo/GO_0005747
http://purl.obolibrary.org/obo/GO_0005750
http://purl.obolibrary.org/obo/GO_0005753
http://purl.obolibrary.org/obo/NCIT_C8384
'endometrioid stromal and related neoplasms' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C8384
http://purl.obolibrary.org/obo/DOID_0111170
http://purl.obolibrary.org/obo/DOID_0111170 EquivalentTo 'autosomal dominant sensory ataxia 1'
http://purl.obolibrary.org/obo/DOID_0111142
http://purl.obolibrary.org/obo/DOID_0111142 EquivalentTo 'oligomeganephronia'
http://purl.obolibrary.org/obo/DOID_0111143
http://purl.obolibrary.org/obo/DOID_0111143 EquivalentTo 'mitochondrial proton-transporting ATP synthase complex deficiency'
http://purl.obolibrary.org/obo/DOID_0111140
http://purl.obolibrary.org/obo/DOID_0111140 EquivalentTo 'X-linked central congenital hypothyroidism with late-onset testicular enlargement'
http://purl.obolibrary.org/obo/DOID_0111141
http://purl.obolibrary.org/obo/DOID_0111141 EquivalentTo 'circadian rhythm sleep disorder, delayed sleep phase type'
http://purl.obolibrary.org/obo/DOID_0111148
http://purl.obolibrary.org/obo/DOID_0111148 EquivalentTo 'isolated ectopia lentis'
http://purl.obolibrary.org/obo/DOID_0111149
http://purl.obolibrary.org/obo/DOID_0111149 EquivalentTo 'ectopia lentis 2, isolated, autosomal recessive'
http://purl.obolibrary.org/obo/DOID_0111146
http://purl.obolibrary.org/obo/DOID_0111146 EquivalentTo 'acquired von willebrand syndrome'
http://purl.obolibrary.org/obo/DOID_0111147
http://purl.obolibrary.org/obo/DOID_0111147 EquivalentTo 'angioimmunoblastic T-cell lymphoma'
http://purl.obolibrary.org/obo/DOID_0111144
http://purl.obolibrary.org/obo/DOID_0111144 EquivalentTo 'preterm premature rupture of the membranes'
http://purl.obolibrary.org/obo/DOID_0111139
http://purl.obolibrary.org/obo/DOID_0111139 EquivalentTo 'mitochondrial complex III deficiency'
http://purl.obolibrary.org/obo/DOID_0111164
http://purl.obolibrary.org/obo/DOID_0111164 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type A'
http://purl.obolibrary.org/obo/DOID_0111165
http://purl.obolibrary.org/obo/DOID_0111165 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency'
http://purl.obolibrary.org/obo/DOID_0111162
http://purl.obolibrary.org/obo/DOID_0111162 EquivalentTo 'nevus, epidermal'
http://purl.obolibrary.org/obo/DOID_0111163
http://purl.obolibrary.org/obo/DOID_0111163 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type B'
http://purl.obolibrary.org/obo/DOID_0111160
http://purl.obolibrary.org/obo/DOID_0111160 EquivalentTo 'camptodactyly-tall stature-scoliosis-hearing loss syndrome'
http://purl.obolibrary.org/obo/DOID_0111161
http://purl.obolibrary.org/obo/DOID_0111161 EquivalentTo 'Crouzon syndrome-acanthosis nigricans syndrome'
http://purl.obolibrary.org/obo/DOID_0111168
http://purl.obolibrary.org/obo/DOID_0111168 EquivalentTo 'Dopa-responsive dystonia due to sepiapterin reductase deficiency'
http://purl.obolibrary.org/obo/DOID_0111169
http://purl.obolibrary.org/obo/DOID_0111169 EquivalentTo 'subcortical band heterotopia'
http://purl.obolibrary.org/obo/DOID_0111166
http://purl.obolibrary.org/obo/DOID_0111166 EquivalentTo 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type C'
http://purl.obolibrary.org/obo/DOID_0111167
http://purl.obolibrary.org/obo/DOID_0111167 EquivalentTo 'Dyggve-Melchior-Clausen disease'
http://purl.obolibrary.org/obo/DOID_0111153
http://purl.obolibrary.org/obo/DOID_0111153 EquivalentTo 'familial congenital mirror movements'
http://purl.obolibrary.org/obo/DOID_0111154
http://purl.obolibrary.org/obo/DOID_0111154 EquivalentTo 'postural orthostatic tachycardia syndrome'
http://purl.obolibrary.org/obo/DOID_0111151
http://purl.obolibrary.org/obo/DOID_0111151 EquivalentTo 'Prinzmetal angina'
http://purl.obolibrary.org/obo/DOID_0111152
http://purl.obolibrary.org/obo/DOID_0111152 EquivalentTo 'multicentric Castleman disease'
http://purl.obolibrary.org/obo/DOID_0111150
http://purl.obolibrary.org/obo/DOID_0111150 EquivalentTo 'ectopia lentis 1, isolated, autosomal dominant'
http://purl.obolibrary.org/obo/DOID_0111159
http://purl.obolibrary.org/obo/DOID_0111159 EquivalentTo 'partial duplication of the long arm of chromosome 4'
http://purl.obolibrary.org/obo/DOID_0111157
http://purl.obolibrary.org/obo/DOID_0111157 EquivalentTo 'Castleman disease'
http://purl.obolibrary.org/obo/DOID_0111158
http://purl.obolibrary.org/obo/DOID_0111158 EquivalentTo 'severe achondroplasia-developmental delay-acanthosis nigricans syndrome'
http://purl.obolibrary.org/obo/DOID_0111155
http://purl.obolibrary.org/obo/DOID_0111155 EquivalentTo 'acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome'
http://purl.obolibrary.org/obo/DOID_0111156
http://purl.obolibrary.org/obo/DOID_0111156 EquivalentTo 'male infertility due to globozoospermia'
http://purl.obolibrary.org/obo/MONDO_0037740
malignant central nervous system mesenchymal, non-meningothelial neoplasm
'malignant central nervous system mesenchymal, non-meningothelial neoplasm' SubClassOf 'malignant soft tissue neoplasm'
'malignant central nervous system mesenchymal, non-meningothelial neoplasm' SubClassOf 'central nervous system cancer'
'malignant central nervous system mesenchymal, non-meningothelial neoplasm' SubClassOf 'central nervous system mesenchymal non-meningothelial tumor'
'malignant central nervous system mesenchymal, non-meningothelial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6758
'malignant central nervous system mesenchymal, non-meningothelial neoplasm' EquivalentTo 'central nervous system mesenchymal non-meningothelial tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
http://purl.obolibrary.org/obo/MONDO_0037742
endometrioid stromal and related neoplasms
'endometrioid stromal and related neoplasms' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C8384
'endometrioid stromal and related neoplasms' SubClassOf 'female reproductive system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0037743
mediastinal soft tissue cancer
'mediastinal soft tissue cancer' SubClassOf 'mediastinal mesenchymal tumor'
'mediastinal soft tissue cancer' SubClassOf 'malignant soft tissue neoplasm'
'mediastinal soft tissue cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6642
'mediastinal soft tissue cancer' EquivalentTo 'mediastinal mesenchymal tumor' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0002097)
'mediastinal soft tissue cancer' SubClassOf 'mediastinal cancer'
http://purl.obolibrary.org/obo/MONDO_0037737
peritoneal solitary fibrous tumor
'peritoneal solitary fibrous tumor' SubClassOf 'peritoneal neoplasm'
'peritoneal solitary fibrous tumor' EquivalentTo 'solitary fibrous tumor' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002358)
'peritoneal solitary fibrous tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C126357
'peritoneal solitary fibrous tumor' SubClassOf 'solitary fibrous tumor'
http://purl.obolibrary.org/obo/MONDO_0037738
cauda equina cancer
'cauda equina cancer' EquivalentTo 'cancer' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0012337)
'cauda equina cancer' SubClassOf 'cauda equina neoplasm'
'cauda equina cancer' SubClassOf 'peripheral nervous system cancer'
'cauda equina cancer' EquivalentTo http://purl.obolibrary.org/obo/SCTID_363477002
http://purl.obolibrary.org/obo/MONDO_0037739
benign neoplasm of cauda equina
'benign neoplasm of cauda equina' SubClassOf 'cauda equina neoplasm'
'benign neoplasm of cauda equina' EquivalentTo http://purl.obolibrary.org/obo/SCTID_92047003
'benign neoplasm of cauda equina' SubClassOf 'nervous system benign neoplasm'
'benign neoplasm of cauda equina' EquivalentTo 'benign neoplasm' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0012337)
http://purl.obolibrary.org/obo/MONDO_0037735
sebaceous gland cancer
'sebaceous gland cancer' EquivalentTo 'cancer' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001821)
'sebaceous gland cancer' SubClassOf 'skin cancer'
'sebaceous gland cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C8409
'sebaceous gland cancer' SubClassOf 'sebaceous gland neoplasm'
http://purl.obolibrary.org/obo/MONDO_0037736
infratentorial neoplasm
'infratentorial neoplasm' SubClassOf 'brain neoplasm'
'infratentorial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3139
http://purl.obolibrary.org/obo/NCIT_C4092
'benign epithelial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4092
http://purl.obolibrary.org/obo/NCIT_C4016
'bone cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4016
http://purl.obolibrary.org/obo/MONDO_0037256
serous neoplasm
'serous neoplasm' SubClassOf 'glandular cell neoplasm'
'serous neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C7074
http://purl.obolibrary.org/obo/MONDO_0037250
childhood testicular neoplasm
'childhood testicular neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C5053
'childhood testicular neoplasm' SubClassOf 'childhood neoplasm'
'childhood testicular neoplasm' EquivalentTo 'neoplasm of testis' and ('has modifier' some http://purl.obolibrary.org/obo/HP_0011463)
'childhood testicular neoplasm' SubClassOf 'neoplasm of testis'
http://purl.obolibrary.org/obo/MONDO_0037251
congestive splenomegaly
'congestive splenomegaly' EquivalentTo http://purl.obolibrary.org/obo/SCTID_19058002
'congestive splenomegaly' SubClassOf 'splenic disease'
'congestive splenomegaly' SubClassOf 'disease has major feature' some http://purl.obolibrary.org/obo/HP_0001744
http://purl.obolibrary.org/obo/MONDO_0037252
thecoma
'thecoma' SubClassOf 'sex cord-stromal tumor'
'thecoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C3405
http://purl.obolibrary.org/obo/MONDO_0037253
ovarian thecoma
'ovarian thecoma' EquivalentTo 'thecoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000992)
'ovarian thecoma' SubClassOf 'thecoma'
'ovarian thecoma' SubClassOf 'ovarian sex cord-stromal tumor'
'ovarian thecoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C66989
http://purl.obolibrary.org/obo/MONDO_0037254
transitional cell neoplasm
'transitional cell neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6783
'transitional cell neoplasm' SubClassOf 'epithelial neoplasm'
http://purl.obolibrary.org/obo/MONDO_0037255
ovarian serous tumor
'ovarian serous tumor' SubClassOf 'ovarian epithelial tumor'
'ovarian serous tumor' SubClassOf 'serous neoplasm'
'ovarian serous tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C8431
'ovarian serous tumor' EquivalentTo 'serous neoplasm' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0000992)
http://purl.obolibrary.org/obo/MONDO_0027766
generalized lipodystrophy
http://purl.obolibrary.org/obo/DOID_0080298 EquivalentTo 'generalized lipodystrophy'
'generalized lipodystrophy' DisjointWith 'partial lipodystrophy'
'generalized lipodystrophy' SubClassOf 'lipodystrophy (disease)'
'generalized lipodystrophy' SubClassOf 'disease has major feature' some http://purl.obolibrary.org/obo/HP_0009064
'generalized lipodystrophy' EquivalentTo 'lipodystrophy (disease)' and ('disease has major feature' some http://purl.obolibrary.org/obo/HP_0009064)
http://purl.obolibrary.org/obo/MONDO_0027767
partial lipodystrophy
'partial lipodystrophy' SubClassOf 'lipodystrophy (disease)'
'generalized lipodystrophy' DisjointWith 'partial lipodystrophy'
http://purl.obolibrary.org/obo/DOID_0080299 EquivalentTo 'partial lipodystrophy'
http://purl.obolibrary.org/obo/MONDO_0037105
lung germ cell tumor
'lung germ cell tumor' SubClassOf 'extragonadal germ cell tumor'
'lung germ cell tumor' EquivalentTo 'germ cell tumor' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002048)
'lung germ cell tumor' SubClassOf 'lung neoplasm'
'lung germ cell tumor' SubClassOf 'rare respiratory disease'
'lung germ cell tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C45636
http://purl.obolibrary.org/obo/MONDO_0027772
lung colloid adenocarcinoma
'lung colloid adenocarcinoma' EquivalentTo 'mucinous adenocarcinoma' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002048)
http://purl.obolibrary.org/obo/DOID_0080304 EquivalentTo 'lung colloid adenocarcinoma'
'lung colloid adenocarcinoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C45512
http://purl.obolibrary.org/obo/DOID_0080303 EquivalentTo 'lung colloid adenocarcinoma'
'lung colloid adenocarcinoma' SubClassOf 'mucinous adenocarcinoma'
'lung colloid adenocarcinoma' SubClassOf 'lung adenocarcinoma'
http://linkedlifedata.com/resource/umls/id/C0020522
http://linkedlifedata.com/resource/umls/id/C0020522 EquivalentTo 'type IV hypersensitivity disease'
http://purl.obolibrary.org/obo/SCTID_363477002
'cauda equina cancer' EquivalentTo http://purl.obolibrary.org/obo/SCTID_363477002
http://purl.obolibrary.org/obo/NCIT_C4454
'lung benign neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4454
http://purl.obolibrary.org/obo/MONDO_0033482
spinocerebellar ataxia 47
'spinocerebellar ataxia 47' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617931
'spinocerebellar ataxia 47' SubClassOf 'cerebellar ataxia'
http://purl.obolibrary.org/obo/MONDO_0033481
spinocerebellar ataxia 46
'spinocerebellar ataxia 46' SubClassOf 'autosomal dominant cerebellar ataxia'
'spinocerebellar ataxia 46' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617770
http://purl.obolibrary.org/obo/DOID_0080288 EquivalentTo 'spinocerebellar ataxia 46'
http://purl.obolibrary.org/obo/MONDO_0033480
spinocerebellar ataxia 45
'spinocerebellar ataxia 45' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617769
'spinocerebellar ataxia 45' SubClassOf 'autosomal dominant cerebellar ataxia'
http://purl.obolibrary.org/obo/DOID_0080287 EquivalentTo 'spinocerebellar ataxia 45'
http://purl.obolibrary.org/obo/MONDO_0033486
leukodystrophy, hypomyelinating, 14
'leukodystrophy, hypomyelinating, 14' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617899
http://purl.obolibrary.org/obo/DOID_0080296 EquivalentTo 'leukodystrophy, hypomyelinating, 14'
'leukodystrophy, hypomyelinating, 14' SubClassOf 'leukodystrophy'
http://purl.obolibrary.org/obo/MONDO_0033485
short-rib thoracic dysplasia 19 with or without polydactyly
'short-rib thoracic dysplasia 19 with or without polydactyly' SubClassOf 'Jeune syndrome'
http://purl.obolibrary.org/obo/DOID_0080295 EquivalentTo 'short-rib thoracic dysplasia 19 with or without polydactyly'
'short-rib thoracic dysplasia 19 with or without polydactyly' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617895
http://purl.obolibrary.org/obo/MONDO_0033483
erythrocytosis, familial, 5
'erythrocytosis, familial, 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617907
'erythrocytosis, familial, 5' SubClassOf 'primary polycythemia'
http://purl.obolibrary.org/obo/DOID_0080290 EquivalentTo 'erythrocytosis, familial, 5'
http://purl.obolibrary.org/obo/MONDO_0033479
spinocerebellar ataxia 44
'spinocerebellar ataxia 44' SubClassOf 'autosomal dominant cerebellar ataxia'
'spinocerebellar ataxia 44' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617691
http://purl.obolibrary.org/obo/DOID_0080286 EquivalentTo 'spinocerebellar ataxia 44'
http://purl.obolibrary.org/obo/MONDO_0033493
fibromatosis, gingival, 5
'fibromatosis, gingival, 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617626
http://purl.obolibrary.org/obo/DOID_0080280 EquivalentTo 'fibromatosis, gingival, 5'
'fibromatosis, gingival, 5' SubClassOf 'gingival fibromatosis'
http://purl.obolibrary.org/obo/MONDO_0033492
coffin-siris syndrome 6
http://purl.obolibrary.org/obo/DOID_0080297 EquivalentTo 'coffin-siris syndrome 6'
'coffin-siris syndrome 6' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'coffin-siris syndrome 6' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617808
http://purl.obolibrary.org/obo/MONDO_0033309
joubert syndrome 32
'joubert syndrome 32' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617757
'joubert syndrome 32' SubClassOf 'Joubert syndrome'
http://purl.obolibrary.org/obo/DOID_0080278 EquivalentTo 'joubert syndrome 32'
http://purl.obolibrary.org/obo/MONDO_0033308
joubert syndrome 30
'joubert syndrome 30' SubClassOf 'Joubert syndrome'
http://purl.obolibrary.org/obo/DOID_0080275 EquivalentTo 'joubert syndrome 30'
'joubert syndrome 30' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617622
http://purl.obolibrary.org/obo/MONDO_0033312
schizophrenia 19
'schizophrenia 19' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617629
http://purl.obolibrary.org/obo/DOID_0080281 EquivalentTo 'schizophrenia 19'
'schizophrenia 19' SubClassOf 'schizophrenia (disease)'
http://purl.obolibrary.org/obo/MONDO_0033311
joubert syndrome 33
'joubert syndrome 33' SubClassOf 'Joubert syndrome'
http://purl.obolibrary.org/obo/DOID_0080279 EquivalentTo 'joubert syndrome 33'
'joubert syndrome 33' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617767
http://purl.obolibrary.org/obo/MONDO_0033310
joubert syndrome 31
http://purl.obolibrary.org/obo/DOID_0080277 EquivalentTo 'joubert syndrome 31'
'joubert syndrome 31' SubClassOf 'Joubert syndrome'
'joubert syndrome 31' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617761
http://purl.obolibrary.org/obo/MONDO_0033361
epileptic encephalopathy, early infantile, 52
'epileptic encephalopathy, early infantile, 52' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617350
'epileptic encephalopathy, early infantile, 52' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033369
epileptic encephalopathy, early infantile, 60
'epileptic encephalopathy, early infantile, 60' SubClassOf 'early infantile epileptic encephalopathy'
'epileptic encephalopathy, early infantile, 60' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617929
http://purl.obolibrary.org/obo/MONDO_0033368
epileptic encephalopathy, early infantile, 59
http://purl.obolibrary.org/obo/DOID_0080291 EquivalentTo 'epileptic encephalopathy, early infantile, 59'
'epileptic encephalopathy, early infantile, 59' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617904
'epileptic encephalopathy, early infantile, 59' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033367
epileptic encephalopathy, early infantile, 58
'epileptic encephalopathy, early infantile, 58' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617830
'epileptic encephalopathy, early infantile, 58' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/DOID_0080285 EquivalentTo 'epileptic encephalopathy, early infantile, 58'
http://purl.obolibrary.org/obo/MONDO_0033366
epileptic encephalopathy, early infantile, 57
'epileptic encephalopathy, early infantile, 57' SubClassOf 'early infantile epileptic encephalopathy'
'epileptic encephalopathy, early infantile, 57' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617771
http://purl.obolibrary.org/obo/DOID_0080284 EquivalentTo 'epileptic encephalopathy, early infantile, 57'
http://purl.obolibrary.org/obo/MONDO_0033365
epileptic encephalopathy, early infantile, 56
http://purl.obolibrary.org/obo/DOID_0080282 EquivalentTo 'epileptic encephalopathy, early infantile, 56'
'epileptic encephalopathy, early infantile, 56' SubClassOf 'early infantile epileptic encephalopathy'
'epileptic encephalopathy, early infantile, 56' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617665
http://purl.obolibrary.org/obo/MONDO_0033364
epileptic encephalopathy, early infantile, 55
'epileptic encephalopathy, early infantile, 55' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/DOID_0080283 EquivalentTo 'epileptic encephalopathy, early infantile, 55'
'epileptic encephalopathy, early infantile, 55' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617599
http://purl.obolibrary.org/obo/MONDO_0033363
epileptic encephalopathy, early infantile, 54
'epileptic encephalopathy, early infantile, 54' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617391
'epileptic encephalopathy, early infantile, 54' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033362
epileptic encephalopathy, early infantile, 53
'epileptic encephalopathy, early infantile, 53' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617389
'epileptic encephalopathy, early infantile, 53' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033372
epileptic encephalopathy, early infantile, 63
'epileptic encephalopathy, early infantile, 63' SubClassOf 'early infantile epileptic encephalopathy'
'epileptic encephalopathy, early infantile, 63' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617976
http://purl.obolibrary.org/obo/MONDO_0033371
epileptic encephalopathy, early infantile, 62
'epileptic encephalopathy, early infantile, 62' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617938
'epileptic encephalopathy, early infantile, 62' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033370
epileptic encephalopathy, early infantile, 61
'epileptic encephalopathy, early infantile, 61' SubClassOf 'early infantile epileptic encephalopathy'
'epileptic encephalopathy, early infantile, 61' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617933
http://purl.obolibrary.org/obo/MONDO_0033375
orofaciodigital syndrome 17
http://purl.obolibrary.org/obo/DOID_0080289 EquivalentTo 'orofaciodigital syndrome 17'
'orofaciodigital syndrome 17' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617926
'orofaciodigital syndrome 17' SubClassOf 'orofaciodigital syndrome'
http://purl.obolibrary.org/obo/MONDO_0033374
epileptic encephalopathy, early infantile, 65
'epileptic encephalopathy, early infantile, 65' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618008
'epileptic encephalopathy, early infantile, 65' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033373
epileptic encephalopathy, early infantile, 64
'epileptic encephalopathy, early infantile, 64' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618004
'epileptic encephalopathy, early infantile, 64' SubClassOf 'early infantile epileptic encephalopathy'
http://purl.obolibrary.org/obo/MONDO_0033199
deafness, autosomal recessive 107
'deafness, autosomal recessive 107' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617639
http://purl.obolibrary.org/obo/DOID_0080262 EquivalentTo 'deafness, autosomal recessive 107'
'deafness, autosomal recessive 107' SubClassOf 'autosomal recessive nonsyndromic deafness'
http://purl.obolibrary.org/obo/MONDO_0033198
deafness, autosomal recessive 106
'deafness, autosomal recessive 106' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617637
'deafness, autosomal recessive 106' SubClassOf 'autosomal recessive nonsyndromic deafness'
http://purl.obolibrary.org/obo/DOID_0080261 EquivalentTo 'deafness, autosomal recessive 106'
http://purl.obolibrary.org/obo/NCIT_C4212
'benign leydig cell tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4212
http://purl.obolibrary.org/obo/MONDO_0033204
ciliary dyskinesia, primary, 37
'ciliary dyskinesia, primary, 37' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617577
http://purl.obolibrary.org/obo/DOID_0080266 EquivalentTo 'ciliary dyskinesia, primary, 37'
'ciliary dyskinesia, primary, 37' SubClassOf 'primary ciliary dyskinesia'
http://purl.obolibrary.org/obo/MONDO_0033203
nephrotic syndrome 14
http://purl.obolibrary.org/obo/DOID_0080265 EquivalentTo 'nephrotic syndrome 14'
'nephrotic syndrome 14' SubClassOf 'familial nephrotic syndrome'
'nephrotic syndrome 14' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617575
http://purl.obolibrary.org/obo/MONDO_0033202
deafness, autosomal recessive 109
'deafness, autosomal recessive 109' SubClassOf 'autosomal recessive nonsyndromic deafness'
'deafness, autosomal recessive 109' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618013
http://purl.obolibrary.org/obo/MONDO_0033201
deafness, autosomal recessive 57
'deafness, autosomal recessive 57' EquivalentTo http://purl.obolibrary.org/obo/OMIM_618003
'deafness, autosomal recessive 57' SubClassOf 'autosomal recessive nonsyndromic deafness'
http://purl.obolibrary.org/obo/MONDO_0033200
deafness, autosomal recessive 108
'deafness, autosomal recessive 108' SubClassOf 'autosomal recessive nonsyndromic deafness'
'deafness, autosomal recessive 108' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617654
http://purl.obolibrary.org/obo/DOID_0080263 EquivalentTo 'deafness, autosomal recessive 108'
http://purl.obolibrary.org/obo/MONDO_0033262
nephrotic syndrome 15
'nephrotic syndrome 15' SubClassOf 'familial nephrotic syndrome'
http://purl.obolibrary.org/obo/DOID_0080271 EquivalentTo 'nephrotic syndrome 15'
'nephrotic syndrome 15' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617609
http://purl.obolibrary.org/obo/MONDO_0033261
deafness, autosomal dominant 34, with or without inflammation
'deafness, autosomal dominant 34, with or without inflammation' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617772
http://purl.obolibrary.org/obo/DOID_0080270 EquivalentTo 'deafness, autosomal dominant 34, with or without inflammation'
'deafness, autosomal dominant 34, with or without inflammation' SubClassOf 'autosomal dominant nonsyndromic deafness'
http://purl.obolibrary.org/obo/MONDO_0033260
deafness, autosomal dominant 73
'deafness, autosomal dominant 73' SubClassOf 'autosomal dominant nonsyndromic deafness'
http://purl.obolibrary.org/obo/DOID_0080269 EquivalentTo 'deafness, autosomal dominant 73'
'deafness, autosomal dominant 73' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617663
http://purl.obolibrary.org/obo/SCTID_123844007
'endometrium neoplasm' EquivalentTo http://purl.obolibrary.org/obo/SCTID_123844007
http://purl.obolibrary.org/obo/NCIT_C4275
'malignant phyllodes tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4275
http://purl.obolibrary.org/obo/NCIT_C4274
'benign phyllodes tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4274
http://purl.obolibrary.org/obo/MONDO_0033259
deafness, autosomal dominant 72
'deafness, autosomal dominant 72' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617606
http://purl.obolibrary.org/obo/DOID_0080268 EquivalentTo 'deafness, autosomal dominant 72'
'deafness, autosomal dominant 72' SubClassOf 'autosomal dominant nonsyndromic deafness'
http://purl.obolibrary.org/obo/MONDO_0033258
deafness, autosomal dominant 71
http://purl.obolibrary.org/obo/DOID_0080267 EquivalentTo 'deafness, autosomal dominant 71'
'deafness, autosomal dominant 71' SubClassOf 'autosomal dominant nonsyndromic deafness'
'deafness, autosomal dominant 71' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617605
http://purl.obolibrary.org/obo/MONDO_0033282
multiple mitochondrial dysfunctions syndrome 5
'multiple mitochondrial dysfunctions syndrome 5' SubClassOf 'fatal multiple mitochondrial dysfunctions syndrome'
http://purl.obolibrary.org/obo/DOID_0080274 EquivalentTo 'multiple mitochondrial dysfunctions syndrome 5'
'multiple mitochondrial dysfunctions syndrome 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617613
http://purl.obolibrary.org/obo/MONDO_0033281
polycystic kidney disease 5
'polycystic kidney disease 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617610
http://purl.obolibrary.org/obo/DOID_0080273 EquivalentTo 'polycystic kidney disease 5'
'polycystic kidney disease 5' SubClassOf 'autosomal dominant polycystic kidney disease'
http://purl.obolibrary.org/obo/MONDO_0033280
nephrotic syndrome 16
'nephrotic syndrome 16' SubClassOf 'familial nephrotic syndrome'
http://purl.obolibrary.org/obo/DOID_0080272 EquivalentTo 'nephrotic syndrome 16'
'nephrotic syndrome 16' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617783
http://purl.obolibrary.org/obo/HP_0100247
http://purl.obolibrary.org/obo/MONDO_0033092
ichthyosis, congenital, autosomal recessive 13
'ichthyosis, congenital, autosomal recessive 13' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617574
http://purl.obolibrary.org/obo/DOID_0080257 EquivalentTo 'ichthyosis, congenital, autosomal recessive 13'
'ichthyosis, congenital, autosomal recessive 13' SubClassOf 'autosomal recessive congenital ichthyosis'
http://purl.obolibrary.org/obo/MONDO_0033091
ichthyosis, congenital, autosomal recessive 14
'ichthyosis, congenital, autosomal recessive 14' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617571
http://purl.obolibrary.org/obo/DOID_0080258 EquivalentTo 'ichthyosis, congenital, autosomal recessive 14'
'ichthyosis, congenital, autosomal recessive 14' SubClassOf 'autosomal recessive congenital ichthyosis'
http://purl.obolibrary.org/obo/MONDO_0033123
exudative vitreoretinopathy 7
http://purl.obolibrary.org/obo/DOID_0080264 EquivalentTo 'exudative vitreoretinopathy 7'
'exudative vitreoretinopathy 7' SubClassOf 'exudative vitreoretinopathy'
'exudative vitreoretinopathy 7' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617572
http://purl.obolibrary.org/obo/MONDO_0033116
spinocerebellar ataxia, autosomal recessive 26
'spinocerebellar ataxia, autosomal recessive 26' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617633
http://purl.obolibrary.org/obo/DOID_0080260 EquivalentTo 'spinocerebellar ataxia, autosomal recessive 26'
'spinocerebellar ataxia, autosomal recessive 26' SubClassOf 'autosomal recessive cerebellar ataxia'
http://purl.obolibrary.org/obo/MONDO_0033115
spinocerebellar ataxia, autosomal recessive 25
'spinocerebellar ataxia, autosomal recessive 25' SubClassOf 'autosomal recessive cerebellar ataxia'
'spinocerebellar ataxia, autosomal recessive 25' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617584
http://purl.obolibrary.org/obo/DOID_0080259 EquivalentTo 'spinocerebellar ataxia, autosomal recessive 25'
http://purl.obolibrary.org/obo/SCTID_293586001
'aspirin allergy' EquivalentTo http://purl.obolibrary.org/obo/SCTID_293586001
http://purl.obolibrary.org/obo/MESH_D007710
http://purl.obolibrary.org/obo/MESH_D007710 EquivalentTo 'Klebsiella infectious disease'
http://purl.obolibrary.org/obo/MONDO_0033009
Galloway-Mowat syndrome 5
'Galloway-Mowat syndrome 5' SubClassOf 'Galloway-Mowat syndrome'
'Galloway-Mowat syndrome 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617731
http://purl.obolibrary.org/obo/DOID_0080247 EquivalentTo 'Galloway-Mowat syndrome 5'
http://purl.obolibrary.org/obo/MONDO_0033008
Galloway-Mowat syndrome 4
http://purl.obolibrary.org/obo/DOID_0080246 EquivalentTo 'Galloway-Mowat syndrome 4'
'Galloway-Mowat syndrome 4' SubClassOf 'Galloway-Mowat syndrome'
'Galloway-Mowat syndrome 4' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617730
http://purl.obolibrary.org/obo/MONDO_0033007
Galloway-Mowat syndrome 3
'Galloway-Mowat syndrome 3' SubClassOf 'Galloway-Mowat syndrome'
'Galloway-Mowat syndrome 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617729
http://purl.obolibrary.org/obo/DOID_0080245 EquivalentTo 'Galloway-Mowat syndrome 3'
http://purl.obolibrary.org/obo/MONDO_0033006
Galloway-Mowat syndrome 2, X-linked
'Galloway-Mowat syndrome 2, X-linked' EquivalentTo http://purl.obolibrary.org/obo/OMIM_301006
'Galloway-Mowat syndrome 2, X-linked' SubClassOf 'Galloway-Mowat syndrome'
http://purl.obolibrary.org/obo/DOID_0080244 EquivalentTo 'Galloway-Mowat syndrome 2, X-linked'
http://purl.obolibrary.org/obo/MONDO_0033005
Galloway-Mowat syndrome 1
'Galloway-Mowat syndrome 1' SubClassOf 'Galloway-Mowat syndrome'
'Galloway-Mowat syndrome 1' EquivalentTo http://purl.obolibrary.org/obo/OMIM_251300
http://purl.obolibrary.org/obo/MONDO_0033004
polycystic kidney disease 4 with or without polycystic liver disease
'polycystic kidney disease 4 with or without polycystic liver disease' EquivalentTo http://purl.obolibrary.org/obo/OMIM_263200
'polycystic kidney disease 4 with or without polycystic liver disease' SubClassOf 'autosomal dominant polycystic kidney disease'
http://purl.obolibrary.org/obo/DOID_0080212 EquivalentTo 'polycystic kidney disease 4 with or without polycystic liver disease'
http://purl.obolibrary.org/obo/MONDO_0033015
erythrokeratodermia variabilis et progressiva 5
http://purl.obolibrary.org/obo/DOID_0080251 EquivalentTo 'erythrokeratodermia variabilis et progressiva 5'
'erythrokeratodermia variabilis et progressiva 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617756
'erythrokeratodermia variabilis et progressiva 5' SubClassOf 'erythrokeratodermia variabilis'
http://purl.obolibrary.org/obo/MONDO_0033014
erythrokeratodermia variabilis et progressiva 4
'erythrokeratodermia variabilis et progressiva 4' SubClassOf 'erythrokeratodermia variabilis'
http://purl.obolibrary.org/obo/DOID_0080250 EquivalentTo 'erythrokeratodermia variabilis et progressiva 4'
'erythrokeratodermia variabilis et progressiva 4' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617526
http://purl.obolibrary.org/obo/MONDO_0033013
erythrokeratodermia variabilis et progressiva 3
http://purl.obolibrary.org/obo/DOID_0080249 EquivalentTo 'erythrokeratodermia variabilis et progressiva 3'
'erythrokeratodermia variabilis et progressiva 3' SubClassOf 'erythrokeratodermia variabilis'
'erythrokeratodermia variabilis et progressiva 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617525
http://purl.obolibrary.org/obo/MONDO_0033012
erythrokeratodermia variabilis et progressiva 2
'erythrokeratodermia variabilis et progressiva 2' SubClassOf 'erythrokeratodermia variabilis'
'erythrokeratodermia variabilis et progressiva 2' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617524
http://purl.obolibrary.org/obo/DOID_0080248 EquivalentTo 'erythrokeratodermia variabilis et progressiva 2'
http://purl.obolibrary.org/obo/MONDO_0033010
erythrokeratodermia variabilis et progressiva 1
'erythrokeratodermia variabilis et progressiva 1' SubClassOf 'erythrokeratodermia variabilis'
'erythrokeratodermia variabilis et progressiva 1' EquivalentTo http://purl.obolibrary.org/obo/OMIM_133200
http://purl.obolibrary.org/obo/MONDO_0033047
Perrault syndrome 6
'Perrault syndrome 6' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617565
http://purl.obolibrary.org/obo/DOID_0080256 EquivalentTo 'Perrault syndrome 6'
'Perrault syndrome 6' SubClassOf 'Perrault syndrome'
http://purl.obolibrary.org/obo/MONDO_0033046
Meier-Gorlin syndrome 8
'Meier-Gorlin syndrome 8' SubClassOf 'Meier-Gorlin syndrome'
'Meier-Gorlin syndrome 8' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617564
http://purl.obolibrary.org/obo/DOID_0080255 EquivalentTo 'Meier-Gorlin syndrome 8'
http://purl.obolibrary.org/obo/MONDO_0033045
orofaciodigital syndrome 16
'orofaciodigital syndrome 16' SubClassOf 'orofaciodigital syndrome'
'orofaciodigital syndrome 16' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617563
http://purl.obolibrary.org/obo/DOID_0080254 EquivalentTo 'orofaciodigital syndrome 16'
http://purl.obolibrary.org/obo/MONDO_0033044
Meckel syndrome 13
http://purl.obolibrary.org/obo/DOID_0080253 EquivalentTo 'Meckel syndrome 13'
'Meckel syndrome 13' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617562
'Meckel syndrome 13' SubClassOf 'Meckel syndrome'
http://purl.obolibrary.org/obo/MONDO_0033043
spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy
'spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy' SubClassOf 'spastic ataxia'
http://purl.obolibrary.org/obo/DOID_0080252 EquivalentTo 'spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy'
'spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617560
http://purl.obolibrary.org/obo/NCIT_C4788
'nervous system cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4788
http://purl.obolibrary.org/obo/NCIT_C66989
'ovarian thecoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C66989
http://purl.obolibrary.org/obo/HP_0002870
http://purl.obolibrary.org/obo/HP_0012205
http://purl.obolibrary.org/obo/ECTO_0001108
http://purl.obolibrary.org/obo/CHEBI_53212
http://purl.obolibrary.org/obo/SCTID_363482009
'pituitary cancer' EquivalentTo http://purl.obolibrary.org/obo/SCTID_363482009
http://purl.obolibrary.org/obo/NCIT_C114346
'type III hypersensitivity disease' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C114346
http://purl.obolibrary.org/obo/GARD_0010012
http://purl.obolibrary.org/obo/GARD_0010012 EquivalentTo 'camptodactyly-tall stature-scoliosis-hearing loss syndrome'
http://purl.obolibrary.org/obo/FOODON_00001792
http://purl.obolibrary.org/obo/NCIT_C114451
'rare childhood malignant neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C114451
http://purl.obolibrary.org/obo/FOODON_00001911
http://purl.obolibrary.org/obo/ICD10_J15.0
http://purl.obolibrary.org/obo/ICD10_J15.0 EquivalentTo 'Klebsiella pneumonia'
http://purl.obolibrary.org/obo/MONDO_0001227ub
chronic tympanitis
'chronic tympanitis' EquivalentTo 'tympanitis' and ('has modifier' some http://purl.obolibrary.org/obo/PATO_0001863)
http://purl.obolibrary.org/obo/COHD_372652 EquivalentTo 'chronic tympanitis'
'chronic tympanitis' SubClassOf 'tympanitis'
'chronic tympanitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_89723004
http://linkedlifedata.com/resource/umls/id/C0395849 EquivalentTo 'chronic tympanitis'
http://purl.obolibrary.org/obo/DOID_11217 EquivalentTo 'chronic tympanitis'
'chronic tympanitis' SubClassOf 'chronic otitis media'
http://purl.obolibrary.org/obo/ICD10_L95.0
http://purl.obolibrary.org/obo/ICD10_L95.0 EquivalentTo 'livedoid vasculopathy'
http://purl.obolibrary.org/obo/SCTID_197850006
'trichomonas cystitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_197850006
http://purl.obolibrary.org/obo/FOODON_00002239
http://purl.obolibrary.org/obo/FOODON_00002244
http://purl.obolibrary.org/obo/OMIMPS_133200
'erythrokeratodermia variabilis' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_133200
http://purl.obolibrary.org/obo/NCBITaxon_570
http://purl.obolibrary.org/obo/FOODON_00002044
http://purl.obolibrary.org/obo/NCIT_C5053
'childhood testicular neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C5053
http://purl.obolibrary.org/obo/NCIT_C120186
'refractory malignant neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C120186
http://purl.obolibrary.org/obo/OMIM_617524
'erythrokeratodermia variabilis et progressiva 2' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617524
http://purl.obolibrary.org/obo/OMIM_617526
'erythrokeratodermia variabilis et progressiva 4' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617526
http://purl.obolibrary.org/obo/OMIM_617525
'erythrokeratodermia variabilis et progressiva 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617525
http://purl.obolibrary.org/obo/OMIM_617575
'nephrotic syndrome 14' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617575
http://purl.obolibrary.org/obo/OMIM_617574
'ichthyosis, congenital, autosomal recessive 13' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617574
http://purl.obolibrary.org/obo/OMIM_617577
'ciliary dyskinesia, primary, 37' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617577
http://purl.obolibrary.org/obo/OMIM_617571
'ichthyosis, congenital, autosomal recessive 14' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617571
http://purl.obolibrary.org/obo/OMIM_617572
'exudative vitreoretinopathy 7' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617572
http://purl.obolibrary.org/obo/OMIM_617564
'Meier-Gorlin syndrome 8' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617564
http://purl.obolibrary.org/obo/OMIM_617563
'orofaciodigital syndrome 16' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617563
http://purl.obolibrary.org/obo/OMIM_617565
'Perrault syndrome 6' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617565
http://purl.obolibrary.org/obo/OMIM_617560
'spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617560
http://purl.obolibrary.org/obo/OMIM_617562
'Meckel syndrome 13' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617562
http://purl.obolibrary.org/obo/OMIM_617654
'deafness, autosomal recessive 108' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617654
http://purl.obolibrary.org/obo/OMIM_617637
'deafness, autosomal recessive 106' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617637
http://purl.obolibrary.org/obo/OMIM_617639
'deafness, autosomal recessive 107' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617639
http://purl.obolibrary.org/obo/OMIM_617633
'spinocerebellar ataxia, autosomal recessive 26' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617633
http://purl.obolibrary.org/obo/OMIM_617635
'intellectual disability, autosomal dominant 47' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617635
http://purl.obolibrary.org/obo/OMIM_617626
'fibromatosis, gingival, 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617626
http://purl.obolibrary.org/obo/OMIM_617629
'schizophrenia 19' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617629
http://purl.obolibrary.org/obo/OMIM_617622
'joubert syndrome 30' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617622
http://purl.obolibrary.org/obo/OMIM_617691
'spinocerebellar ataxia 44' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617691
http://purl.obolibrary.org/obo/OMIM_617663
'deafness, autosomal dominant 73' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617663
http://purl.obolibrary.org/obo/OMIM_617665
'epileptic encephalopathy, early infantile, 56' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617665
http://purl.obolibrary.org/obo/OMIM_617609
'nephrotic syndrome 15' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617609
http://purl.obolibrary.org/obo/OMIM_617613
'multiple mitochondrial dysfunctions syndrome 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617613
http://purl.obolibrary.org/obo/OMIM_617610
'polycystic kidney disease 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617610
http://purl.obolibrary.org/obo/OMIM_617605
'deafness, autosomal dominant 71' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617605
http://purl.obolibrary.org/obo/OMIM_617606
'deafness, autosomal dominant 72' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617606
http://purl.obolibrary.org/obo/OMIM_617601
'intellectual disability, autosomal dominant 46' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617601
http://purl.obolibrary.org/obo/OMIM_617600
'intellectual disability, autosomal dominant 45' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617600
http://purl.obolibrary.org/obo/OMIM_617599
'epileptic encephalopathy, early infantile, 55' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617599
http://purl.obolibrary.org/obo/OMIM_617584
'spinocerebellar ataxia, autosomal recessive 25' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617584
http://purl.obolibrary.org/obo/OMIM_617773
'intellectual disability, autosomal recessive 61' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617773
http://purl.obolibrary.org/obo/OMIM_617772
'deafness, autosomal dominant 34, with or without inflammation' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617772
http://purl.obolibrary.org/obo/OMIM_617771
'epileptic encephalopathy, early infantile, 57' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617771
http://purl.obolibrary.org/obo/OMIM_617770
'spinocerebellar ataxia 46' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617770
http://purl.obolibrary.org/obo/OMIM_617769
'spinocerebellar ataxia 45' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617769
http://purl.obolibrary.org/obo/OMIM_617767
'joubert syndrome 33' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617767
http://purl.obolibrary.org/obo/OMIM_617761
'joubert syndrome 31' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617761
http://purl.obolibrary.org/obo/UBERON_0003532
http://purl.obolibrary.org/obo/OMIM_617757
'joubert syndrome 32' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617757
http://purl.obolibrary.org/obo/OMIM_617756
'erythrokeratodermia variabilis et progressiva 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617756
http://purl.obolibrary.org/obo/OMIM_617751
'intellectual disability, autosomal dominant 48' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617751
http://purl.obolibrary.org/obo/OMIM_617752
'intellectual disability, autosomal dominant 49' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617752
http://purl.obolibrary.org/obo/OMIM_617799
'intellectual disability, autosomal dominant 54' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617799
http://purl.obolibrary.org/obo/OMIM_617798
'intellectual disability, autosomal dominant 53' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617798
http://purl.obolibrary.org/obo/OMIM_617796
'intellectual disability, autosomal dominant 52' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617796
http://purl.obolibrary.org/obo/OMIM_617788
'intellectual disability, autosomal dominant 51' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617788
http://purl.obolibrary.org/obo/OMIM_617787
'intellectual disability, autosomal dominant 50' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617787
http://purl.obolibrary.org/obo/OMIM_617783
'nephrotic syndrome 16' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617783
http://purl.obolibrary.org/obo/OMIM_617729
'Galloway-Mowat syndrome 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617729
http://purl.obolibrary.org/obo/OMIM_617731
'Galloway-Mowat syndrome 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617731
http://purl.obolibrary.org/obo/OMIM_617730
'Galloway-Mowat syndrome 4' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617730
http://purl.obolibrary.org/obo/OMIM_617899
'leukodystrophy, hypomyelinating, 14' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617899
http://purl.obolibrary.org/obo/OMIM_617895
'short-rib thoracic dysplasia 19 with or without polydactyly' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617895
http://purl.obolibrary.org/obo/OMIM_617882
'charcot-marie-tooth disease, dominant intermediate G' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617882
http://purl.obolibrary.org/obo/OMIM_617871
'retinitis pigmentosa 81' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617871
http://purl.obolibrary.org/obo/OMIM_617866
'short-rib thoracic dysplasia 18 with polydactyly' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617866
http://purl.obolibrary.org/obo/OMIM_617808
'coffin-siris syndrome 6' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617808
http://purl.obolibrary.org/obo/OMIM_617854
'intellectual disability, autosomal dominant 56' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617854
http://purl.obolibrary.org/obo/OMIM_617839
'amyotrophic lateral sclerosis type 23' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617839
http://purl.obolibrary.org/obo/OMIM_617831
'intellectual disability, autosomal dominant 55, with seizures' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617831
http://purl.obolibrary.org/obo/OMIM_617830
'epileptic encephalopathy, early infantile, 58' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617830
http://purl.obolibrary.org/obo/OMIM_617929
'epileptic encephalopathy, early infantile, 60' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617929
http://purl.obolibrary.org/obo/OMIM_617931
'spinocerebellar ataxia 47' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617931
http://purl.obolibrary.org/obo/OMIM_617933
'epileptic encephalopathy, early infantile, 61' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617933
http://purl.obolibrary.org/obo/OMIM_617926
'orofaciodigital syndrome 17' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617926
http://purl.obolibrary.org/obo/OMIM_617907
'erythrocytosis, familial, 5' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617907
http://purl.obolibrary.org/obo/OMIM_617904
'epileptic encephalopathy, early infantile, 59' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617904
http://purl.obolibrary.org/obo/OMIM_617976
'epileptic encephalopathy, early infantile, 63' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617976
http://purl.obolibrary.org/obo/OMIM_617938
'epileptic encephalopathy, early infantile, 62' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617938
http://purl.obolibrary.org/obo/ICD10_J15
http://purl.obolibrary.org/obo/ICD10_J15 EquivalentTo 'pneumonia'
http://purl.obolibrary.org/obo/SCTID_402397006
'autoimmune urticaria' EquivalentTo http://purl.obolibrary.org/obo/SCTID_402397006
http://purl.obolibrary.org/obo/MONDO_0029042
obsolete ureteropelvic junction obstruction
http://purl.obolibrary.org/obo/OMIM_617403
'autosomal recessive cutis laxa type 2d' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617403
http://purl.obolibrary.org/obo/OMIM_617402
'autosomal recessive cutis laxa type 2c' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617402
http://purl.obolibrary.org/obo/OMIM_617350
'epileptic encephalopathy, early infantile, 52' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617350
http://purl.obolibrary.org/obo/OMIM_617391
'epileptic encephalopathy, early infantile, 54' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617391
http://purl.obolibrary.org/obo/OMIM_617389
'epileptic encephalopathy, early infantile, 53' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617389
http://purl.obolibrary.org/obo/SCTID_35089004
'trichomonas vaginitis urogenital infection' EquivalentTo http://purl.obolibrary.org/obo/SCTID_35089004
http://purl.obolibrary.org/obo/MONDO_0030922
intellectual disability, autosomal dominant 56
'intellectual disability, autosomal dominant 56' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617854
http://purl.obolibrary.org/obo/DOID_0080226 EquivalentTo 'intellectual disability, autosomal dominant 56'
'intellectual disability, autosomal dominant 56' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0030921
intellectual disability, autosomal dominant 55, with seizures
'intellectual disability, autosomal dominant 55, with seizures' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'intellectual disability, autosomal dominant 55, with seizures' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617831
http://purl.obolibrary.org/obo/DOID_0080227 EquivalentTo 'intellectual disability, autosomal dominant 55, with seizures'
http://purl.obolibrary.org/obo/MONDO_0030920
intellectual disability, autosomal dominant 54
'intellectual disability, autosomal dominant 54' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'intellectual disability, autosomal dominant 54' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617799
http://purl.obolibrary.org/obo/DOID_0080230 EquivalentTo 'intellectual disability, autosomal dominant 54'
http://purl.obolibrary.org/obo/NCIT_C45636
'lung germ cell tumor' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C45636
http://purl.obolibrary.org/obo/MONDO_0030911
intellectual disability, autosomal dominant 46
'intellectual disability, autosomal dominant 46' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'intellectual disability, autosomal dominant 46' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617601
http://purl.obolibrary.org/obo/DOID_0080237 EquivalentTo 'intellectual disability, autosomal dominant 46'
http://purl.obolibrary.org/obo/MONDO_0030910
intellectual disability, autosomal dominant 45
'intellectual disability, autosomal dominant 45' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617600
'intellectual disability, autosomal dominant 45' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0080236 EquivalentTo 'intellectual disability, autosomal dominant 45'
http://purl.obolibrary.org/obo/MONDO_0030913
intellectual disability, autosomal dominant 48
'intellectual disability, autosomal dominant 48' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0080235 EquivalentTo 'intellectual disability, autosomal dominant 48'
'intellectual disability, autosomal dominant 48' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617751
http://purl.obolibrary.org/obo/MONDO_0030912
intellectual disability, autosomal dominant 47
'intellectual disability, autosomal dominant 47' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'intellectual disability, autosomal dominant 47' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617635
http://purl.obolibrary.org/obo/DOID_0080238 EquivalentTo 'intellectual disability, autosomal dominant 47'
http://purl.obolibrary.org/obo/MONDO_0030919
intellectual disability, autosomal dominant 53
'intellectual disability, autosomal dominant 53' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0080228 EquivalentTo 'intellectual disability, autosomal dominant 53'
'intellectual disability, autosomal dominant 53' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617798
http://purl.obolibrary.org/obo/MONDO_0030918
intellectual disability, autosomal dominant 52
http://purl.obolibrary.org/obo/DOID_0080231 EquivalentTo 'intellectual disability, autosomal dominant 52'
'intellectual disability, autosomal dominant 52' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617796
'intellectual disability, autosomal dominant 52' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0030915
intellectual disability, autosomal recessive 61
'intellectual disability, autosomal recessive 61' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617773
http://purl.obolibrary.org/obo/DOID_0080239 EquivalentTo 'intellectual disability, autosomal recessive 61'
'intellectual disability, autosomal recessive 61' SubClassOf 'autosomal recessive non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0030914
intellectual disability, autosomal dominant 49
'intellectual disability, autosomal dominant 49' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617752
http://purl.obolibrary.org/obo/DOID_0080234 EquivalentTo 'intellectual disability, autosomal dominant 49'
'intellectual disability, autosomal dominant 49' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0030917
intellectual disability, autosomal dominant 51
http://purl.obolibrary.org/obo/DOID_0080232 EquivalentTo 'intellectual disability, autosomal dominant 51'
'intellectual disability, autosomal dominant 51' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'intellectual disability, autosomal dominant 51' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617788
http://purl.obolibrary.org/obo/MONDO_0030916
intellectual disability, autosomal dominant 50
http://purl.obolibrary.org/obo/DOID_0080233 EquivalentTo 'intellectual disability, autosomal dominant 50'
'intellectual disability, autosomal dominant 50' SubClassOf 'autosomal dominant non-syndromic intellectual disability'
'intellectual disability, autosomal dominant 50' EquivalentTo http://purl.obolibrary.org/obo/OMIM_617787
http://purl.obolibrary.org/obo/MONDO_0030908
intellectual disability, X-linked, syndromic, 35
'intellectual disability, X-linked, syndromic, 35' SubClassOf 'X-linked syndromic intellectual disability'
'intellectual disability, X-linked, syndromic, 35' EquivalentTo http://purl.obolibrary.org/obo/OMIM_300998
http://purl.obolibrary.org/obo/DOID_0080241 EquivalentTo 'intellectual disability, X-linked, syndromic, 35'
http://purl.obolibrary.org/obo/MONDO_0030907
intellectual disability, X-linked 106
'intellectual disability, X-linked 106' EquivalentTo http://purl.obolibrary.org/obo/OMIM_300997
http://purl.obolibrary.org/obo/DOID_0080240 EquivalentTo 'intellectual disability, X-linked 106'
'intellectual disability, X-linked 106' SubClassOf 'non-syndromic X-linked intellectual disability'
http://purl.obolibrary.org/obo/MONDO_0030909
intellectual disability, X-linked, syndromic, Houge type
'intellectual disability, X-linked, syndromic, Houge type' SubClassOf 'X-linked syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0080242 EquivalentTo 'intellectual disability, X-linked, syndromic, Houge type'
'intellectual disability, X-linked, syndromic, Houge type' EquivalentTo http://purl.obolibrary.org/obo/OMIM_301008
http://purl.obolibrary.org/obo/MONDO_0030906
trichomonas tenax infectious disease
'trichomonas tenax infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_43075
'trichomonas tenax infectious disease' SubClassOf 'trichomoniasis'
'trichomonas tenax infectious disease' EquivalentTo 'disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_43075)
http://purl.obolibrary.org/obo/DOID_0050270 EquivalentTo 'trichomonas tenax infectious disease'
http://purl.obolibrary.org/obo/MONDO_0030702
autoimmune atherosclerosis
'autoimmune atherosclerosis' EquivalentTo 'atherosclerosis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune atherosclerosis' SubClassOf 'atherosclerosis'
http://purl.obolibrary.org/obo/DOID_0040096 EquivalentTo 'autoimmune atherosclerosis'
'autoimmune atherosclerosis' SubClassOf 'autoimmune disease of cardiovascular system'
http://purl.obolibrary.org/obo/MONDO_0030701
autoimmune cardiomyopathy
'autoimmune cardiomyopathy' SubClassOf 'autoimmune disease of cardiovascular system'
'autoimmune cardiomyopathy' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/DOID_0040095 EquivalentTo 'autoimmune cardiomyopathy'
'autoimmune cardiomyopathy' SubClassOf 'cardiomyopathy'
'autoimmune cardiomyopathy' EquivalentTo 'cardiomyopathy' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune cardiomyopathy' SubClassOf 'autoimmune disease of musculoskeletal system'
http://purl.obolibrary.org/obo/MONDO_0030703
autoimmune vasculitis
'autoimmune vasculitis' EquivalentTo 'vasculitis' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune vasculitis' SubClassOf 'autoimmune disease of cardiovascular system'
http://purl.obolibrary.org/obo/DOID_0040097 EquivalentTo 'autoimmune vasculitis'
'autoimmune vasculitis' SubClassOf 'vasculitis'
'autoimmune vasculitis' SubClassOf 'rare immune disease'
http://purl.obolibrary.org/obo/MONDO_0030700
autoimmune glomerulonephritis
'autoimmune glomerulonephritis' SubClassOf 'rare urogenital disease'
'autoimmune glomerulonephritis' SubClassOf 'autoimmune disease of urogenital tract'
'autoimmune glomerulonephritis' SubClassOf 'rare immune disease'
'autoimmune glomerulonephritis' EquivalentTo 'glomerulonephritis (disease)' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
http://purl.obolibrary.org/obo/DOID_0040094 EquivalentTo 'autoimmune glomerulonephritis'
'autoimmune glomerulonephritis' SubClassOf 'glomerulonephritis (disease)'
http://purl.obolibrary.org/obo/MONDO_0030706
trichomonas cystitis
'trichomonas cystitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35405
'trichomonas cystitis' SubClassOf 'cystitis'
'trichomonas cystitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_197850006
'trichomonas cystitis' EquivalentTo 'cystitis' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
'trichomonas cystitis' SubClassOf 'trichomonas vaginitis urogenital infection'
http://purl.obolibrary.org/obo/MONDO_0030705
trichomonas prostatitis
'trichomonas prostatitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35176
'trichomonas prostatitis' SubClassOf 'prostatitis (disease)'
'trichomonas prostatitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_71590000
'trichomonas prostatitis' EquivalentTo 'prostatitis (disease)' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
'trichomonas prostatitis' SubClassOf 'trichomoniasis'
'trichomonas prostatitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722
http://purl.obolibrary.org/obo/MONDO_0030708
trichomonas cervicitis
'trichomonas cervicitis' EquivalentTo 'cervicitis (disease)' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
'trichomonas cervicitis' SubClassOf 'trichomoniasis'
'trichomonas cervicitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722
'trichomonas cervicitis' SubClassOf 'cervicitis (disease)'
'trichomonas cervicitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35588
http://purl.obolibrary.org/obo/MONDO_0030707
trichomonas balanoposthitis
'trichomonas balanoposthitis' SubClassOf 'balanoposthitis'
'trichomonas balanoposthitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35406
'trichomonas balanoposthitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722
'trichomonas balanoposthitis' EquivalentTo 'balanoposthitis' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
'trichomonas balanoposthitis' SubClassOf 'trichomoniasis'
http://purl.obolibrary.org/obo/MONDO_0030720
trichomonal vulvovaginitis
'trichomonal vulvovaginitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_81598001
'trichomonal vulvovaginitis' SubClassOf 'vulvovaginitis'
'trichomonal vulvovaginitis' SubClassOf 'trichomonas vaginitis urogenital infection'
'trichomonal vulvovaginitis' EquivalentTo 'vulvovaginitis' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5722)
http://purl.obolibrary.org/obo/GARD_0008702
http://purl.obolibrary.org/obo/GARD_0008702 EquivalentTo 'atypical hemolytic-uremic syndrome'
http://purl.obolibrary.org/obo/SCTID_233609002
'pneumonia caused by chlamydia' EquivalentTo http://purl.obolibrary.org/obo/SCTID_233609002
http://purl.obolibrary.org/obo/MONDO_0030603
Klebsiella infectious disease
http://purl.obolibrary.org/obo/MESH_D007710 EquivalentTo 'Klebsiella infectious disease'
'Klebsiella infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_570
'Klebsiella infectious disease' SubClassOf 'disease'
'Klebsiella infectious disease' EquivalentTo 'disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_570)
http://purl.obolibrary.org/obo/MONDO_0030602
Klebsiella pneumonia
http://purl.obolibrary.org/obo/DOID_13272 EquivalentTo 'Klebsiella pneumonia'
'Klebsiella pneumonia' SubClassOf 'bacterial pneumonia'
http://purl.obolibrary.org/obo/ICD10_J15.0 EquivalentTo 'Klebsiella pneumonia'
'Klebsiella pneumonia' SubClassOf 'Klebsiella infectious disease'
'Klebsiella pneumonia' EquivalentTo 'pneumonia' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_570)
'Klebsiella pneumonia' EquivalentTo http://purl.obolibrary.org/obo/SCTID_64479007
http://purl.obolibrary.org/obo/MONDO_0030604
cystic partially differentiated nephroblastoma
'cystic partially differentiated nephroblastoma' SubClassOf 'childhood kidney wilms tumor'
http://purl.obolibrary.org/obo/DOID_7571 EquivalentTo 'cystic partially differentiated nephroblastoma'
'cystic partially differentiated nephroblastoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6897
'cystic partially differentiated nephroblastoma' SubClassOf 'childhood multilocular cystic kidney neoplasm'
http://purl.obolibrary.org/obo/DOID_0040100
http://purl.obolibrary.org/obo/DOID_0040100 EquivalentTo 'insulin autoimmune syndrome'
http://purl.obolibrary.org/obo/DOID_0040087
http://purl.obolibrary.org/obo/DOID_0040087 EquivalentTo 'autoimmune neuropathy'
http://purl.obolibrary.org/obo/DOID_0040085
http://purl.obolibrary.org/obo/DOID_0040085 EquivalentTo 'bacterial infectious disease with sepsis'
http://purl.obolibrary.org/obo/DOID_0040084
http://purl.obolibrary.org/obo/DOID_0040084 EquivalentTo 'streptococcal pneumonia'
http://purl.obolibrary.org/obo/DOID_0040089
http://purl.obolibrary.org/obo/DOID_0040089 EquivalentTo 'autoimmune optic neuritis'
http://purl.obolibrary.org/obo/DOID_0040088
http://purl.obolibrary.org/obo/DOID_0040088 EquivalentTo 'autoimmune uveitis'
http://purl.obolibrary.org/obo/DOID_0040083
http://purl.obolibrary.org/obo/DOID_0040083 EquivalentTo 'pneumonia caused by chlamydia'
http://purl.obolibrary.org/obo/DOID_0040041
http://purl.obolibrary.org/obo/DOID_0040041 EquivalentTo 'isocyanate induced asthma'
http://purl.obolibrary.org/obo/DOID_0040002
http://purl.obolibrary.org/obo/DOID_0040002 EquivalentTo 'aspirin allergy'
http://purl.obolibrary.org/obo/DOID_0040001
http://purl.obolibrary.org/obo/DOID_0040001 EquivalentTo 'shrimp allergy'
http://purl.obolibrary.org/obo/DOID_13276
http://purl.obolibrary.org/obo/DOID_13276 EquivalentTo 'Mycoplasma pneumoniae pneumonia'
http://purl.obolibrary.org/obo/DOID_13272
http://purl.obolibrary.org/obo/DOID_13272 EquivalentTo 'Klebsiella pneumonia'
http://purl.obolibrary.org/obo/DOID_0040098
http://purl.obolibrary.org/obo/DOID_0040098 EquivalentTo 'pemphigoid gestationis'
http://purl.obolibrary.org/obo/DOID_0040097
http://purl.obolibrary.org/obo/DOID_0040097 EquivalentTo 'autoimmune vasculitis'
http://purl.obolibrary.org/obo/DOID_0040096
http://purl.obolibrary.org/obo/DOID_0040096 EquivalentTo 'autoimmune atherosclerosis'
http://purl.obolibrary.org/obo/DOID_0040095
http://purl.obolibrary.org/obo/DOID_0040095 EquivalentTo 'autoimmune cardiomyopathy'
http://purl.obolibrary.org/obo/DOID_0040099
http://purl.obolibrary.org/obo/DOID_0040099 EquivalentTo 'livedoid vasculopathy'
http://purl.obolibrary.org/obo/DOID_0040090
http://purl.obolibrary.org/obo/DOID_0040090 EquivalentTo 'autoimmune gastritis'
http://purl.obolibrary.org/obo/DOID_0040094
http://purl.obolibrary.org/obo/DOID_0040094 EquivalentTo 'autoimmune glomerulonephritis'
http://purl.obolibrary.org/obo/DOID_0040093
http://purl.obolibrary.org/obo/DOID_0040093 EquivalentTo 'drug-induced lupus erythematosus'
http://purl.obolibrary.org/obo/DOID_0040091
http://purl.obolibrary.org/obo/DOID_0040091 EquivalentTo 'autoimmune pancreatitis'
http://purl.obolibrary.org/obo/NCIT_C123907
'childhood malignant kidney neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C123907
http://purl.obolibrary.org/obo/NCIT_C45512
'lung colloid adenocarcinoma' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C45512
http://purl.obolibrary.org/obo/MONDO_0025598
pneumonia caused by chlamydia
'pneumonia caused by chlamydia' EquivalentTo http://purl.obolibrary.org/obo/SCTID_233609002
http://purl.obolibrary.org/obo/DOID_0040083 EquivalentTo 'pneumonia caused by chlamydia'
'pneumonia caused by chlamydia' SubClassOf 'chlamydia trachomatis infectious disease'
'pneumonia caused by chlamydia' SubClassOf 'bacterial pneumonia'
'pneumonia caused by chlamydia' EquivalentTo 'pneumonia' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_810)
http://purl.obolibrary.org/obo/NCIT_C6758
'malignant central nervous system mesenchymal, non-meningothelial neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6758
http://purl.obolibrary.org/obo/NCIT_C35406
'trichomonas balanoposthitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35406
http://purl.obolibrary.org/obo/NCIT_C35405
'trichomonas cystitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35405
http://purl.obolibrary.org/obo/NCIT_C6783
'transitional cell neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6783
http://purl.obolibrary.org/obo/MONDO_0025513
autoimmune urticaria
'autoimmune urticaria' EquivalentTo 'urticaria (disease)' and ('disease arises from feature' some http://purl.obolibrary.org/obo/HP_0002960)
'autoimmune urticaria' SubClassOf 'rare urticaria'
'autoimmune urticaria' SubClassOf 'autoimmune disease with skin involvement'
'autoimmune urticaria' EquivalentTo http://purl.obolibrary.org/obo/SCTID_402397006
http://purl.obolibrary.org/obo/MONDO_0025512
type II hypersensitivity reaction disease
'type II hypersensitivity reaction disease' EquivalentTo 'disease' and ('disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445)
'type II hypersensitivity reaction disease' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0002445
'type II hypersensitivity reaction disease' SubClassOf 'autoimmune disease'
'type II hypersensitivity reaction disease' EquivalentTo http://www.ebi.ac.uk/efo/EFO_0005809
http://purl.obolibrary.org/obo/MONDO_0025514
livedoid vasculopathy
http://purl.obolibrary.org/obo/ICD10_L95.0 EquivalentTo 'livedoid vasculopathy'
'livedoid vasculopathy' SubClassOf 'vasculitis'
'livedoid vasculopathy' EquivalentTo http://purl.obolibrary.org/obo/SCTID_238762002
'livedoid vasculopathy' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0003532
'livedoid vasculopathy' SubClassOf 'rare skin disease'
'livedoid vasculopathy' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000979
http://purl.obolibrary.org/obo/GARD_0012784 EquivalentTo 'livedoid vasculopathy'
'livedoid vasculopathy' SubClassOf 'disorder of anatomical region'
http://purl.obolibrary.org/obo/DOID_0040099 EquivalentTo 'livedoid vasculopathy'
'livedoid vasculopathy' EquivalentTo 'vasculitis' and ('disease has feature' some http://purl.obolibrary.org/obo/HP_0000979)
http://purl.obolibrary.org/obo/MONDO_0025517
shrimp allergy
'shrimp allergy' SubClassOf 'crustacean allergy'
'shrimp allergy' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00002239)
http://purl.obolibrary.org/obo/DOID_0040001 EquivalentTo 'shrimp allergy'
'shrimp allergy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/FOODON_00002239
http://purl.obolibrary.org/obo/MONDO_0025518
aspirin allergy
'aspirin allergy' SubClassOf 'drug allergy'
'aspirin allergy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/CHEBI_15365
'aspirin allergy' EquivalentTo 'allergic disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/CHEBI_15365)
'aspirin allergy' EquivalentTo http://purl.obolibrary.org/obo/SCTID_293586001
http://purl.obolibrary.org/obo/DOID_0040002 EquivalentTo 'aspirin allergy'
http://purl.obolibrary.org/obo/SCTID_71590000
'trichomonas prostatitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_71590000
http://purl.obolibrary.org/obo/MONDO_0025556
isocyanate induced asthma
'isocyanate induced asthma' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/CHEBI_53212
'isocyanate induced asthma' SubClassOf 'allergic asthma'
http://purl.obolibrary.org/obo/DOID_0040041 EquivalentTo 'isocyanate induced asthma'
'isocyanate induced asthma' EquivalentTo 'asthma' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/CHEBI_53212)
'isocyanate induced asthma' EquivalentTo http://purl.obolibrary.org/obo/SCTID_404808000
http://purl.obolibrary.org/obo/NCIT_C6642
'mediastinal soft tissue cancer' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C6642
http://purl.obolibrary.org/obo/SCTID_19058002
'congestive splenomegaly' EquivalentTo http://purl.obolibrary.org/obo/SCTID_19058002
http://purl.obolibrary.org/obo/NCIT_C35588
'trichomonas cervicitis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35588
http://purl.obolibrary.org/obo/NCIT_C35749
'axillary neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35749
http://purl.obolibrary.org/obo/NCIT_C35750
'benign axillary neoplasm' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C35750
http://purl.obolibrary.org/obo/DOID_0050269
http://purl.obolibrary.org/obo/DOID_0050269 EquivalentTo 'trichomonas vaginitis urogenital infection'
http://purl.obolibrary.org/obo/DOID_0050270
http://purl.obolibrary.org/obo/DOID_0050270 EquivalentTo 'trichomonas tenax infectious disease'
http://purl.obolibrary.org/obo/OMIM_300998
'intellectual disability, X-linked, syndromic, 35' EquivalentTo http://purl.obolibrary.org/obo/OMIM_300998
http://purl.obolibrary.org/obo/OMIM_300997
'intellectual disability, X-linked 106' EquivalentTo http://purl.obolibrary.org/obo/OMIM_300997
http://purl.obolibrary.org/obo/GARD_0006240
http://purl.obolibrary.org/obo/GARD_0006240 EquivalentTo 'atypical hemolytic-uremic syndrome'
http://linkedlifedata.com/resource/umls/id/C0021070
http://linkedlifedata.com/resource/umls/id/C0021070 EquivalentTo 'hypersensitivity reaction type IV disease'
http://www.orpha.net/ORDO/Orphanet_2190
'congenital hydronephrosis' EquivalentTo http://www.orpha.net/ORDO/Orphanet_2190
http://purl.obolibrary.org/obo/MONDO_0001227
chronic tympanitis
http://purl.obolibrary.org/obo/COHD_372652 EquivalentTo 'chronic tympanitis'
'chronic tympanitis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_89723004
'chronic tympanitis' SubClassOf 'tympanitis'
http://linkedlifedata.com/resource/umls/id/C0395849 EquivalentTo 'chronic tympanitis'
http://purl.obolibrary.org/obo/DOID_11217 EquivalentTo 'chronic tympanitis'