50 156 0 http://purl.obolibrary.org/obo/MONDO_0033555 immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia 'immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0979261 http://purl.obolibrary.org/obo/MONDO_0033554 immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia 'immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia' SubClassOf http://purl.obolibrary.org/obo/MONDO_0979261 http://purl.obolibrary.org/obo/MONDO_0008436 Sneddon syndrome 'Sneddon syndrome' SubClassOf 'hereditary skin disorder' http://purl.obolibrary.org/obo/MONDO_0008226 periodontitis, aggressive 1 'periodontitis, aggressive 1' SubClassOf 'chronic periodontitis' 'periodontitis, aggressive 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0980757 http://purl.obolibrary.org/obo/MONDO_0011712 van der Woude syndrome 2 'van der Woude syndrome 2' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0060707 Ververi-Brady syndrome 1 'Ververi-Brady syndrome 1' SubClassOf 'Ververi-Brady syndrome' http://purl.obolibrary.org/obo/MONDO_0011690 Camurati-Engelmann disease, type 2 'Camurati-Engelmann disease, type 2' SubClassOf 'hereditary disease' 'Camurati-Engelmann disease, type 2' SubClassOf 'syndromic disease' 'Camurati-Engelmann disease, type 2' SubClassOf 'Camurati-Engelmann disease' http://purl.obolibrary.org/obo/MONDO_0035423 triglyceride deposit cardiomyovasculopathy 'triglyceride deposit cardiomyovasculopathy' SubClassOf 'neutral lipid storage disease' 'triglyceride deposit cardiomyovasculopathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0979259 http://purl.obolibrary.org/obo/MONDO_0004169 premenstrual tension 'premenstrual tension' SubClassOf 'female reproductive system disorder' 'premenstrual tension' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060204 http://purl.obolibrary.org/obo/MONDO_0006809 intracranial embolism 'intracranial embolism' SubClassOf 'cerebrovascular disorder' 'intracranial embolism' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060198 http://purl.obolibrary.org/obo/MONDO_0006686 brain stem infarction 'brain stem infarction' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060198 http://purl.obolibrary.org/obo/MONDO_0018585 pediatric arterial ischemic stroke 'pediatric arterial ischemic stroke' SubClassOf 'stroke disorder' 'pediatric arterial ischemic stroke' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060198 http://purl.obolibrary.org/obo/MONDO_0008769 neuronal ceroid lipofuscinosis 2 'neuronal ceroid lipofuscinosis 2' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 2' SubClassOf 'late infantile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 2' SubClassOf 'neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0008768 ceroid lipofuscinosis, neuronal, 6B (Kufs type) 'ceroid lipofuscinosis, neuronal, 6B (Kufs type)' SubClassOf 'adult neuronal ceroid lipofuscinosis' 'ceroid lipofuscinosis, neuronal, 6B (Kufs type)' SubClassOf 'neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0008767 neuronal ceroid lipofuscinosis 3 'neuronal ceroid lipofuscinosis 3' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 3' SubClassOf 'neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0976261 congenital disorder of glycosylation type 1EE with or without immunodeficiency 'congenital disorder of glycosylation type 1EE with or without immunodeficiency' SubClassOf 'congenital disorder of glycosylation' 'congenital disorder of glycosylation type 1EE with or without immunodeficiency' SubClassOf 'disorder of protein N-glycosylation' http://purl.obolibrary.org/obo/MONDO_0014003 developmental and epileptic encephalopathy, 15 'developmental and epileptic encephalopathy, 15' SubClassOf 'congenital nervous system disorder' 'developmental and epileptic encephalopathy, 15' SubClassOf http://purl.obolibrary.org/obo/MONDO_0979317 http://purl.obolibrary.org/obo/MONDO_0100489 Graves disease, susceptibility to, 1 'Graves disease, susceptibility to, 1' SubClassOf 'autoimmune thyroid disease, susceptibility to' 'Graves disease, susceptibility to, 1' SubClassOf 'inherited disease susceptibility' http://purl.obolibrary.org/obo/MONDO_0004586 rheumatoid lung disease 'rheumatoid lung disease' SubClassOf 'autoimmune disease' 'rheumatoid lung disease' SubClassOf 'rheumatoid arthritis' http://purl.obolibrary.org/obo/MONDO_0100289 Goldmann-Favre syndrome 'Goldmann-Favre syndrome' SubClassOf 'vitreoretinal degeneration' 'Goldmann-Favre syndrome' SubClassOf 'enhanced S-cone syndrome' http://purl.obolibrary.org/obo/MONDO_0016377 Pitt-Hopkins-like syndrome 'Pitt-Hopkins-like syndrome' SubClassOf 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability' 'Pitt-Hopkins-like syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0980732 http://purl.obolibrary.org/obo/MONDO_0012612 intellectual disability, autosomal recessive 12 'intellectual disability, autosomal recessive 12' SubClassOf http://purl.obolibrary.org/obo/MONDO_0979317 'intellectual disability, autosomal recessive 12' SubClassOf 'congenital nervous system disorder' http://purl.obolibrary.org/obo/MONDO_0009062 cystic fibrosis-gastritis-megaloblastic anemia syndrome 'cystic fibrosis-gastritis-megaloblastic anemia syndrome' SubClassOf 'hereditary disease' 'cystic fibrosis-gastritis-megaloblastic anemia syndrome' SubClassOf 'cystic fibrosis' http://purl.obolibrary.org/obo/MONDO_0012589 Pitt-Hopkins syndrome 'Pitt-Hopkins syndrome' SubClassOf 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability' 'Pitt-Hopkins syndrome' SubClassOf 'hereditary disease' 'Pitt-Hopkins syndrome' SubClassOf http://purl.obolibrary.org/obo/MONDO_0980732 http://purl.obolibrary.org/obo/MONDO_0012391 neuronal ceroid lipofuscinosis 8 northern epilepsy variant 'neuronal ceroid lipofuscinosis 8 northern epilepsy variant' SubClassOf 'juvenile myoclonic epilepsy' http://purl.obolibrary.org/obo/MONDO_0012400 cortical dysplasia-focal epilepsy syndrome 'cortical dysplasia-focal epilepsy syndrome' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0012414 neuronal ceroid lipofuscinosis 10 'neuronal ceroid lipofuscinosis 10' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 10' SubClassOf 'adult neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 10' SubClassOf 'late infantile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 10' SubClassOf 'neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0012051 periodontitis, aggressive, 2 'periodontitis, aggressive, 2' SubClassOf 'chronic periodontitis' 'periodontitis, aggressive, 2' SubClassOf http://purl.obolibrary.org/obo/MONDO_0980757 http://purl.obolibrary.org/obo/MONDO_0002679 cerebral infarction 'cerebral infarction' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060198 http://purl.obolibrary.org/obo/MONDO_0968978 aplasia cutis-enamel dysplasia syndrome 'aplasia cutis-enamel dysplasia syndrome' SubClassOf 'hereditary disease' 'aplasia cutis-enamel dysplasia syndrome' SubClassOf 'syndromic disease' 'aplasia cutis-enamel dysplasia syndrome' SubClassOf 'Mendelian neurodevelopmental disorder' 'aplasia cutis-enamel dysplasia syndrome' SubClassOf 'syndromic intellectual disability' http://purl.obolibrary.org/obo/MONDO_0010830 neuronal ceroid lipofuscinosis 8 'neuronal ceroid lipofuscinosis 8' SubClassOf 'late infantile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 8' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'neuronal ceroid lipofuscinosis 8' SubClassOf 'neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0020143 cerebral lipidosis with dementia 'cerebral lipidosis with dementia' SubClassOf 'hereditary dementia' http://purl.obolibrary.org/obo/MONDO_0010417 syndromic X-linked intellectual disability Najm type 'syndromic X-linked intellectual disability Najm type' SubClassOf 'central nervous system malformation' 'syndromic X-linked intellectual disability Najm type' SubClassOf 'X-linked syndromic intellectual disability' 'syndromic X-linked intellectual disability Najm type' SubClassOf 'central nervous system malformation' 'syndromic X-linked intellectual disability Najm type' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060192 http://purl.obolibrary.org/obo/MONDO_0010318 FG syndrome 4 'FG syndrome 4' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060192 http://purl.obolibrary.org/obo/MONDO_0010138 thyrotoxicosis 'thyrotoxicosis' SubClassOf 'Graves disease' 'thyrotoxicosis' SubClassOf 'hyperthyroidism' http://purl.obolibrary.org/obo/MONDO_0010178 congenital bilateral aplasia of vas deferens from CFTR mutation 'congenital bilateral aplasia of vas deferens from CFTR mutation' SubClassOf http://purl.obolibrary.org/obo/MONDO_7770004 http://purl.obolibrary.org/obo/MONDO_0005364 Graves disease 'Graves disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060200 http://purl.obolibrary.org/obo/MONDO_0005264 transient ischemic attack 'transient ischemic attack' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060198 http://purl.obolibrary.org/obo/MONDO_0005099 subarachnoid hemorrhage 'subarachnoid hemorrhage' SubClassOf 'neurovascular disorder' 'subarachnoid hemorrhage' SubClassOf 'brain disorder' 'subarachnoid hemorrhage' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060199 http://purl.obolibrary.org/obo/MONDO_0019508 van der Woude syndrome 'van der Woude syndrome' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0007333 van der Woude syndrome 1 'van der Woude syndrome 1' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0013088 follicular lymphoma, susceptibility to, 1 'follicular lymphoma, susceptibility to, 1' SubClassOf 'hereditary neoplastic syndrome' 'follicular lymphoma, susceptibility to, 1' SubClassOf http://purl.obolibrary.org/obo/MONDO_0980759 http://purl.obolibrary.org/obo/MONDO_0017819 atypical dentin dysplasia due to SMOC2 deficiency 'atypical dentin dysplasia due to SMOC2 deficiency' SubClassOf 'dentin dysplasia type I' 'atypical dentin dysplasia due to SMOC2 deficiency' SubClassOf 'dentin dysplasia type I' http://purl.obolibrary.org/obo/MONDO_0001836 amenorrhea 'amenorrhea' SubClassOf 'female reproductive system disorder' 'amenorrhea' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060204 http://purl.obolibrary.org/obo/MONDO_0013792 intracerebral hemorrhage 'intracerebral hemorrhage' SubClassOf 'cerebrovascular disorder' 'intracerebral hemorrhage' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060199 http://purl.obolibrary.org/obo/MONDO_0011144 ceroid lipofuscinosis, neuronal, 6A 'ceroid lipofuscinosis, neuronal, 6A' SubClassOf 'ceroid lipofuscinosis, neuronal, 6B (Kufs type)' 'ceroid lipofuscinosis, neuronal, 6A' SubClassOf 'neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0859371 rhabdomyolysis, susceptibility to, 1 'rhabdomyolysis, susceptibility to, 1' SubClassOf 'inherited disease susceptibility' 'rhabdomyolysis, susceptibility to, 1' SubClassOf 'rhabdomyolysis, susceptibility to' http://purl.obolibrary.org/obo/MONDO_0013690 Pitt-Hopkins-like syndrome 2 'Pitt-Hopkins-like syndrome 2' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0001252 Plummer disease 'Plummer disease' SubClassOf 'hyperthyroidism' 'Plummer disease' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060200 http://purl.obolibrary.org/obo/MONDO_0003837 TSH producing pituitary tumor 'TSH producing pituitary tumor' SubClassOf 'thyroid tumor' 'TSH producing pituitary tumor' SubClassOf http://purl.obolibrary.org/obo/MONDO_1060201 http://purl.obolibrary.org/obo/MONDO_7770003 cystic fibrosis-related diabetes 'cystic fibrosis-related diabetes' SubClassOf 'diabetes mellitus' http://purl.obolibrary.org/obo/MONDO_7770005 cystic fibrosis-related liver disease 'cystic fibrosis-related liver disease' SubClassOf 'liver disorder' http://purl.obolibrary.org/obo/MONDO_7770004 CFTR-related disorder 'CFTR-related disorder' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0975920 RNASEH2B-related hereditary spastic paraplegia 'RNASEH2B-related hereditary spastic paraplegia' SubClassOf 'hereditary spastic paraplegia' http://purl.obolibrary.org/obo/MONDO_0975919 IFIH1-related hereditary spastic paraplegia 'IFIH1-related hereditary spastic paraplegia' SubClassOf 'hereditary spastic paraplegia' http://purl.obolibrary.org/obo/MONDO_0700391 autoinflammation and autoimmunity with immune dysregulation 1 'autoinflammation and autoimmunity with immune dysregulation 1' SubClassOf 'autoimmune interstitial lung disease-arthritis syndrome' http://purl.obolibrary.org/obo/MONDO_0700390 follicular lymphoma, susceptibility to, 2 'follicular lymphoma, susceptibility to, 2' SubClassOf 'follicular lymphoma, susceptibility to' http://purl.obolibrary.org/obo/MONDO_0700393 idiopathic triglyceride deposit cardiomyovasculopathy 'idiopathic triglyceride deposit cardiomyovasculopathy' SubClassOf 'triglyceride deposit cardiomyovasculopathy' http://purl.obolibrary.org/obo/MONDO_0700392 autoinflammation and autoimmunity with immune dysregulation 2 'autoinflammation and autoimmunity with immune dysregulation 2' SubClassOf 'autoimmune interstitial lung disease-arthritis syndrome' http://purl.obolibrary.org/obo/MONDO_0700388 cardiac conduction disease with or without dilated cardiomyopathy 1 'cardiac conduction disease with or without dilated cardiomyopathy 1' SubClassOf 'cardiac conduction disease with or without cardiomyoopathy' http://purl.obolibrary.org/obo/MONDO_0700387 dentin dysplasia, type IB 'dentin dysplasia, type IB' SubClassOf 'dentin dysplasia type I' http://purl.obolibrary.org/obo/MONDO_0700389 cardiac conduction disease with or without cardiomyopathy 2 'cardiac conduction disease with or without cardiomyopathy 2' SubClassOf 'cardiac conduction disease with or without cardiomyoopathy' http://purl.obolibrary.org/obo/MONDO_0700386 enhanced S-cone syndrome 2 'enhanced S-cone syndrome 2' SubClassOf 'enhanced S-cone syndrome' http://purl.obolibrary.org/obo/MONDO_0700385 Camurati-Engelmann disease type 1 'Camurati-Engelmann disease type 1' SubClassOf 'Camurati-Engelmann disease' http://purl.obolibrary.org/obo/MONDO_1060197 congenital heart disease with heterotaxy syndrome 'congenital heart disease with heterotaxy syndrome' SubClassOf 'syndromic congenital heart disease' http://purl.obolibrary.org/obo/MONDO_1060192 CASK-related intellectual disability 'CASK-related intellectual disability' SubClassOf 'X-linked syndromic intellectual disability' http://purl.obolibrary.org/obo/MONDO_1060193 X-linked intellectual disability with or without nystagmus 'X-linked intellectual disability with or without nystagmus' SubClassOf 'CASK-related intellectual disability' http://purl.obolibrary.org/obo/MONDO_1060198 ischemic stroke 'ischemic stroke' SubClassOf 'stroke disorder' http://purl.obolibrary.org/obo/MONDO_1060199 hemorrhagic stroke 'hemorrhagic stroke' SubClassOf 'stroke disorder' http://purl.obolibrary.org/obo/MONDO_1060204 menstrual disorder 'menstrual disorder' SubClassOf 'female reproductive system disorder' http://purl.obolibrary.org/obo/MONDO_1060205 dysmenorrhea 'dysmenorrhea' SubClassOf 'menstrual disorder' http://purl.obolibrary.org/obo/MONDO_1060202 toxic thyroid adenoma 'toxic thyroid adenoma' SubClassOf 'follicular thyroid adenoma' 'toxic thyroid adenoma' SubClassOf 'primary hyperthyroidism' http://purl.obolibrary.org/obo/MONDO_1060203 hypothalamic hyperthyroidism 'hypothalamic hyperthyroidism' SubClassOf 'secondary hyperthyroidism' http://purl.obolibrary.org/obo/MONDO_1060200 primary hyperthyroidism 'primary hyperthyroidism' SubClassOf 'hyperthyroidism' http://purl.obolibrary.org/obo/MONDO_1060201 secondary hyperthyroidism 'secondary hyperthyroidism' SubClassOf 'hyperthyroidism' http://purl.obolibrary.org/obo/MONDO_1060208 primary amenorrhea 'primary amenorrhea' SubClassOf 'amenorrhea' http://purl.obolibrary.org/obo/MONDO_1060209 secondary amenorrhea 'secondary amenorrhea' SubClassOf 'amenorrhea' http://purl.obolibrary.org/obo/MONDO_1060206 primary dysmenorrhea 'primary dysmenorrhea' SubClassOf 'dysmenorrhea' http://purl.obolibrary.org/obo/MONDO_1060207 secondary dysmenorrhea 'secondary dysmenorrhea' SubClassOf 'dysmenorrhea' http://purl.obolibrary.org/obo/MONDO_1060210 functional hypothalamic amenorrhea 'functional hypothalamic amenorrhea' SubClassOf 'secondary amenorrhea' http://purl.obolibrary.org/obo/MONDO_0978310 adenomatoid tumour of the peritoneum 'adenomatoid tumour of the peritoneum' SubClassOf 'adenomatoid tumor' http://purl.obolibrary.org/obo/MONDO_0978312 isolated anal canal duplication 'isolated anal canal duplication' SubClassOf 'anorectal malformation' http://purl.obolibrary.org/obo/MONDO_0978307 isolated jejuno-ileal duplication 'isolated jejuno-ileal duplication' SubClassOf 'small intestine duplication' http://purl.obolibrary.org/obo/MONDO_0978306 isolated duodenal duplication 'isolated duodenal duplication' SubClassOf 'small intestine duplication' http://purl.obolibrary.org/obo/MONDO_0980974 craniosynostosis-scoliosis syndrome 'craniosynostosis-scoliosis syndrome' SubClassOf 'hereditary disease' 'craniosynostosis-scoliosis syndrome' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0980973 STAD syndrome 'STAD syndrome' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0980972 hypotrichosis 16 'hypotrichosis 16' SubClassOf 'hypotrichosis' http://purl.obolibrary.org/obo/MONDO_0980971 charcot-marie-tooth disease, axonal, type 2MM 'charcot-marie-tooth disease, axonal, type 2MM' SubClassOf 'Charcot-Marie-Tooth disease' http://purl.obolibrary.org/obo/MONDO_0980970 mitochondrial complex 4 deficiency, nuclear type 25 'mitochondrial complex 4 deficiency, nuclear type 25' SubClassOf 'mitochondrial complex IV deficiency, nuclear-type' http://purl.obolibrary.org/obo/MONDO_0980969 Charcot-Marie-Tooth disease, axonal, type 2LL 'Charcot-Marie-Tooth disease, axonal, type 2LL' SubClassOf 'Charcot-Marie-Tooth disease' http://purl.obolibrary.org/obo/MONDO_0980968 neurodevelopmental disorder with seizures, hypotonia, and variable spasticity 'neurodevelopmental disorder with seizures, hypotonia, and variable spasticity' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980967 mitochondrial dna depletion syndrome 14A (encephalomyopathic type) 'mitochondrial dna depletion syndrome 14A (encephalomyopathic type)' SubClassOf 'mitochondrial DNA depletion syndrome' http://purl.obolibrary.org/obo/MONDO_0980966 developmental and epileptic encephalopathy 121 'developmental and epileptic encephalopathy 121' SubClassOf 'genetic developmental and epileptic encephalopathy' http://purl.obolibrary.org/obo/MONDO_0980965 neurodevelopmental disorder with congenital cardiac defects and variable renal and ocular abnormalities 'neurodevelopmental disorder with congenital cardiac defects and variable renal and ocular abnormalities' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980964 oocyte/zygote/embryo maturation arrest 25 'oocyte/zygote/embryo maturation arrest 25' SubClassOf 'inherited oocyte maturation defect' http://purl.obolibrary.org/obo/MONDO_0980963 Charcot-Marie-Tooth disease, axonal, type 2KK 'Charcot-Marie-Tooth disease, axonal, type 2KK' SubClassOf 'Charcot-Marie-Tooth disease' http://purl.obolibrary.org/obo/MONDO_0980939 basal ganglia calcification, idiopathic, 11, autosomal recessive 'basal ganglia calcification, idiopathic, 11, autosomal recessive' SubClassOf 'bilateral striopallidodentate calcinosis' http://purl.obolibrary.org/obo/MONDO_0980938 osteopetrosis, autosomal dominant 4 'osteopetrosis, autosomal dominant 4' SubClassOf 'autosomal dominant osteopetrosis' http://purl.obolibrary.org/obo/MONDO_0980937 oculopharyngodistal myopathy 5 'oculopharyngodistal myopathy 5' SubClassOf 'oculopharyngodistal myopathy' http://purl.obolibrary.org/obo/MONDO_0980936 neutropenia, severe congenital, 12, autosomal recessive 'neutropenia, severe congenital, 12, autosomal recessive' SubClassOf 'severe congenital neutropenia' http://purl.obolibrary.org/obo/MONDO_0980935 microcephaly, progressive, with simplified gyral pattern and cerebellar hypoplasia 'microcephaly, progressive, with simplified gyral pattern and cerebellar hypoplasia' SubClassOf 'microcephaly' http://purl.obolibrary.org/obo/MONDO_0980949 Moyamoya disease 8 'Moyamoya disease 8' SubClassOf 'Moyamoya disease' http://purl.obolibrary.org/obo/MONDO_0980948 developmental and epileptic encephalopathy 120 'developmental and epileptic encephalopathy 120' SubClassOf 'genetic developmental and epileptic encephalopathy' http://purl.obolibrary.org/obo/MONDO_0980947 neurodevelopmental disorder with spasticity, thin corpus callosum, and decreased brain white matter 'neurodevelopmental disorder with spasticity, thin corpus callosum, and decreased brain white matter' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980942 intellectual developmental disorder with seizures and dysmorphic facies 'intellectual developmental disorder with seizures and dysmorphic facies' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0980941 neurodevelopmental disorder with speech delay, movement abnormalities, and seizures 'neurodevelopmental disorder with speech delay, movement abnormalities, and seizures' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980940 neurodevelopmental disorder with hypotonia, epilepsy, and absent speech 'neurodevelopmental disorder with hypotonia, epilepsy, and absent speech' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0979898 Dursun-Ozgul neurodevelopmental syndrome 'Dursun-Ozgul neurodevelopmental syndrome' SubClassOf 'syndromic disease' 'Dursun-Ozgul neurodevelopmental syndrome' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0979897 congenital myopathy 27 'congenital myopathy 27' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0979899 spondyloepiphyseal dysplasia, Holling type 'spondyloepiphyseal dysplasia, Holling type' SubClassOf 'spondyloepiphyseal dysplasia' http://purl.obolibrary.org/obo/MONDO_0979288 combined immunodeficiency due to dimerization defective IKAROS mutation 'combined immunodeficiency due to dimerization defective IKAROS mutation' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0979292 primary vitreoretinal large b-cell lymphoma 'primary vitreoretinal large b-cell lymphoma' SubClassOf 'diffuse large B-cell lymphoma' 'primary vitreoretinal large b-cell lymphoma' SubClassOf 'immune system cancer' 'primary vitreoretinal large b-cell lymphoma' SubClassOf 'eye lymphoma' http://purl.obolibrary.org/obo/MONDO_0979291 3q26q28 deletion syndrome '3q26q28 deletion syndrome' SubClassOf 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability' '3q26q28 deletion syndrome' SubClassOf 'partial deletion of the long arm of chromosome 3' http://purl.obolibrary.org/obo/MONDO_0979290 late-onset combined immunodeficiency due to ICOSL deficiency 'late-onset combined immunodeficiency due to ICOSL deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0979273 ADAR-related hereditary spastic paraplegia 'ADAR-related hereditary spastic paraplegia' SubClassOf 'hereditary spastic paraplegia' http://purl.obolibrary.org/obo/MONDO_0979271 congenital intrahepatic arterioportal fistula 'congenital intrahepatic arterioportal fistula' SubClassOf 'congenital arteriovenous fistula' http://purl.obolibrary.org/obo/MONDO_0979284 acinar cystic transformation of the pancreas 'acinar cystic transformation of the pancreas' SubClassOf 'pancreas disorder' http://purl.obolibrary.org/obo/MONDO_0979287 sickle cell-beta plus-thalassemia 'sickle cell-beta plus-thalassemia' SubClassOf 'sickle cell-beta-thalassemia disease syndrome' http://purl.obolibrary.org/obo/MONDO_0979286 sickle cell-beta zero-thalassemia 'sickle cell-beta zero-thalassemia' SubClassOf 'sickle cell-beta-thalassemia disease syndrome' http://purl.obolibrary.org/obo/MONDO_0979281 giant omphalocele 'giant omphalocele' SubClassOf 'omphalocele' http://purl.obolibrary.org/obo/MONDO_0979280 pure squamous carcinoma of the urothelial tract 'pure squamous carcinoma of the urothelial tract' SubClassOf 'urothelial carcinoma' 'pure squamous carcinoma of the urothelial tract' SubClassOf 'squamous cell carcinoma' http://purl.obolibrary.org/obo/MONDO_0979282 small omphalocele 'small omphalocele' SubClassOf 'omphalocele' http://purl.obolibrary.org/obo/MONDO_0979259 triglyceride deposit cardiomyovasculopathy 'triglyceride deposit cardiomyovasculopathy' SubClassOf 'neutral lipid storage disease' http://purl.obolibrary.org/obo/MONDO_0979258 cerebral proliferative angiopathy 'cerebral proliferative angiopathy' SubClassOf 'vascular malformation' http://purl.obolibrary.org/obo/MONDO_0979257 isolated anogenital granulomatosis 'isolated anogenital granulomatosis' SubClassOf 'inflammatory disease' http://purl.obolibrary.org/obo/MONDO_0979261 RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome 'RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome' SubClassOf 'syndromic disease' 'RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0979368 juvenile neuronal ceroid lipofuscinosis 6 'juvenile neuronal ceroid lipofuscinosis 6' SubClassOf 'ceroid lipofuscinosis, neuronal, 6A' 'juvenile neuronal ceroid lipofuscinosis 6' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0979367 late infantile neuronal ceroid lipofuscinosis 6 'late infantile neuronal ceroid lipofuscinosis 6' SubClassOf 'ceroid lipofuscinosis, neuronal, 6A' http://purl.obolibrary.org/obo/MONDO_0979373 juvenile neuronal ceroid lipofuscinosis 10 'juvenile neuronal ceroid lipofuscinosis 10' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'juvenile neuronal ceroid lipofuscinosis 10' SubClassOf 'neuronal ceroid lipofuscinosis 10' http://purl.obolibrary.org/obo/MONDO_0979372 late infantile neuronal ceroid lipofuscinosis 10 'late infantile neuronal ceroid lipofuscinosis 10' SubClassOf 'neuronal ceroid lipofuscinosis 10' http://purl.obolibrary.org/obo/MONDO_0979371 congenital neuronal ceroid lipofuscinosis 10 'congenital neuronal ceroid lipofuscinosis 10' SubClassOf 'neuronal ceroid lipofuscinosis 10' 'congenital neuronal ceroid lipofuscinosis 10' SubClassOf 'congenital nervous system disorder' http://purl.obolibrary.org/obo/MONDO_0979370 late infantile neuronal ceroid lipofuscinosis 8 'late infantile neuronal ceroid lipofuscinosis 8' SubClassOf 'neuronal ceroid lipofuscinosis 8' http://purl.obolibrary.org/obo/MONDO_0979348 late infantile neuronal ceroid lipofuscinosis 5 'late infantile neuronal ceroid lipofuscinosis 5' SubClassOf 'neuronal ceroid lipofuscinosis 5' http://purl.obolibrary.org/obo/MONDO_0979347 protracted juvenile neuronal ceroid lipofuscinosis 3 'protracted juvenile neuronal ceroid lipofuscinosis 3' SubClassOf 'neuronal ceroid lipofuscinosis 3' http://purl.obolibrary.org/obo/MONDO_0979349 juvenile neuronal ceroid lipofuscinosis 5 'juvenile neuronal ceroid lipofuscinosis 5' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'juvenile neuronal ceroid lipofuscinosis 5' SubClassOf 'neuronal ceroid lipofuscinosis 5' http://purl.obolibrary.org/obo/MONDO_0979344 late infantile neuronal ceroid lipofuscinosis 2 'late infantile neuronal ceroid lipofuscinosis 2' SubClassOf 'neuronal ceroid lipofuscinosis 2' http://purl.obolibrary.org/obo/MONDO_0979343 infantile neuronal ceroid lipofuscinosis 2 'infantile neuronal ceroid lipofuscinosis 2' SubClassOf 'neuronal ceroid lipofuscinosis 2' 'infantile neuronal ceroid lipofuscinosis 2' SubClassOf 'infantile neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0979346 juvenile neuronal ceroid lipofuscinosis 3 'juvenile neuronal ceroid lipofuscinosis 3' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'juvenile neuronal ceroid lipofuscinosis 3' SubClassOf 'neuronal ceroid lipofuscinosis 3' http://purl.obolibrary.org/obo/MONDO_0979345 juvenile neuronal ceroid lipofuscinosis 2 'juvenile neuronal ceroid lipofuscinosis 2' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'juvenile neuronal ceroid lipofuscinosis 2' SubClassOf 'neuronal ceroid lipofuscinosis 2' http://purl.obolibrary.org/obo/MONDO_0979350 adult neuronal ceroid lipofuscinosis 5 'adult neuronal ceroid lipofuscinosis 5' SubClassOf 'neuronal ceroid lipofuscinosis 5' 'adult neuronal ceroid lipofuscinosis 5' SubClassOf 'adult neuronal ceroid lipofuscinosis' http://purl.obolibrary.org/obo/MONDO_0979353 2p25.3 microduplication syndrome '2p25.3 microduplication syndrome' SubClassOf 'syndromic intellectual disability' '2p25.3 microduplication syndrome' SubClassOf 'partial duplication of the short arm of chromosome 2' http://purl.obolibrary.org/obo/MONDO_0979359 TARDBP-related predominantly upper-limb distal myopathy 'TARDBP-related predominantly upper-limb distal myopathy' SubClassOf 'autosomal dominant distal myopathy' http://purl.obolibrary.org/obo/MONDO_0979355 homozygous hemoglobin O Arab disease 'homozygous hemoglobin O Arab disease' SubClassOf 'inherited hemoglobinopathy' http://purl.obolibrary.org/obo/MONDO_0979354 sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variant 'sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variant' SubClassOf 'sickle cell disease' http://purl.obolibrary.org/obo/MONDO_0979357 idiopathic chronic pancreatitis 'idiopathic chronic pancreatitis' SubClassOf 'chronic pancreatitis' http://purl.obolibrary.org/obo/MONDO_0979356 autosomal recessive hereditary chronic pancreatitis 'autosomal recessive hereditary chronic pancreatitis' SubClassOf 'hereditary chronic pancreatitis' http://purl.obolibrary.org/obo/MONDO_0979362 calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy 'calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy' SubClassOf 'autosomal dominant distal myopathy' http://purl.obolibrary.org/obo/MONDO_0979361 asymetric thumb-handgrip weakness-distal myopathy 'asymetric thumb-handgrip weakness-distal myopathy' SubClassOf 'autosomal dominant distal myopathy' http://purl.obolibrary.org/obo/MONDO_0979360 ADNP-related blepharophimosis-intellectual disability syndrome 'ADNP-related blepharophimosis-intellectual disability syndrome' SubClassOf 'blepharophimosis - intellectual disability syndrome' 'ADNP-related blepharophimosis-intellectual disability syndrome' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0979326 Fontan-associated liver disease 'Fontan-associated liver disease' SubClassOf 'hepatic vascular disorder' http://purl.obolibrary.org/obo/MONDO_0979325 annular erythema of infancy 'annular erythema of infancy' SubClassOf 'dermis disorder' http://purl.obolibrary.org/obo/MONDO_0979328 immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency 'immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency' SubClassOf 'inborn error of immunity' http://purl.obolibrary.org/obo/MONDO_0979327 combined immunodeficiency with low Ig due to BCL10 deficiency 'combined immunodeficiency with low Ig due to BCL10 deficiency' SubClassOf 'combined immunodeficiency' 'combined immunodeficiency with low Ig due to BCL10 deficiency' SubClassOf 'immunodeficiency 37' http://purl.obolibrary.org/obo/MONDO_0979323 carotid web 'carotid web' SubClassOf 'arterial disorder' http://purl.obolibrary.org/obo/MONDO_0979337 necrotizing myositis 'necrotizing myositis' SubClassOf 'necrotizing soft tissue infection' http://purl.obolibrary.org/obo/MONDO_0979339 infantile neuronal ceroid lipofuscinosis 1 'infantile neuronal ceroid lipofuscinosis 1' SubClassOf 'infantile neuronal ceroid lipofuscinosis' 'infantile neuronal ceroid lipofuscinosis 1' SubClassOf 'neuronal ceroid lipofuscinosis 1' http://purl.obolibrary.org/obo/MONDO_0979335 fibro-adipose vascular anomaly 'fibro-adipose vascular anomaly' SubClassOf 'vascular malformation' http://purl.obolibrary.org/obo/MONDO_0979334 necrotizing cellulitis 'necrotizing cellulitis' SubClassOf 'necrotizing soft tissue infection' http://purl.obolibrary.org/obo/MONDO_0979340 late infantile neuronal ceroid lipofuscinosis 1 'late infantile neuronal ceroid lipofuscinosis 1' SubClassOf 'neuronal ceroid lipofuscinosis 1' http://purl.obolibrary.org/obo/MONDO_0979342 adult neuronal ceroid lipofuscinosis 1 'adult neuronal ceroid lipofuscinosis 1' SubClassOf 'adult neuronal ceroid lipofuscinosis' 'adult neuronal ceroid lipofuscinosis 1' SubClassOf 'neuronal ceroid lipofuscinosis 1' http://purl.obolibrary.org/obo/MONDO_0979341 juvenile neuronal ceroid lipofuscinosis 1 'juvenile neuronal ceroid lipofuscinosis 1' SubClassOf 'juvenile neuronal ceroid lipofuscinosis' 'juvenile neuronal ceroid lipofuscinosis 1' SubClassOf 'neuronal ceroid lipofuscinosis 1' http://purl.obolibrary.org/obo/MONDO_0979307 emergomycosis 'emergomycosis' SubClassOf 'fungal infectious disease' http://purl.obolibrary.org/obo/MONDO_0979300 PPARG-associated congenital generalized lipodystrophy 'PPARG-associated congenital generalized lipodystrophy' SubClassOf 'Berardinelli-Seip congenital lipodystrophy' http://purl.obolibrary.org/obo/MONDO_0979319 congenital peritoneal encapsulation 'congenital peritoneal encapsulation' SubClassOf 'digestive system disorder' 'congenital peritoneal encapsulation' SubClassOf 'disorder of development or morphogenesis' http://purl.obolibrary.org/obo/MONDO_0979315 combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to IKBKA deficiency 'combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to IKBKA deficiency' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0979317 ST3GAL3-congenital disorder of glycosylation 'ST3GAL3-congenital disorder of glycosylation' SubClassOf 'disorder of protein N-glycosylation' http://purl.obolibrary.org/obo/MONDO_0979316 early-onset combined immunodeficiency with low ig due to dominant negative IKAROS mutation 'early-onset combined immunodeficiency with low ig due to dominant negative IKAROS mutation' SubClassOf 'combined immunodeficiency' http://purl.obolibrary.org/obo/MONDO_0979310 lymphoepithelial cyst of the pancreas 'lymphoepithelial cyst of the pancreas' SubClassOf 'pancreas disorder' http://purl.obolibrary.org/obo/MONDO_0980732 Pitt-Hopkins or Pitt-Hopkins-like syndrome 'Pitt-Hopkins or Pitt-Hopkins-like syndrome' SubClassOf 'hereditary disease' 'Pitt-Hopkins or Pitt-Hopkins-like syndrome' SubClassOf 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability' http://purl.obolibrary.org/obo/MONDO_0980749 apolipoprotein A-II deficiency 'apolipoprotein A-II deficiency' SubClassOf 'hypoalphalipoproteinemia' http://purl.obolibrary.org/obo/MONDO_0980748 intellectual developmental disorder, autosomal dominant 77 'intellectual developmental disorder, autosomal dominant 77' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0980747 brain small vessel disease 2B, autosomal recessive 'brain small vessel disease 2B, autosomal recessive' SubClassOf 'familial porencephaly' http://purl.obolibrary.org/obo/MONDO_0980746 intellectual developmental disorder, autosomal recessive 84 'intellectual developmental disorder, autosomal recessive 84' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0980715 cardiac conduction disease with or without cardiomyoopathy 'cardiac conduction disease with or without cardiomyoopathy' SubClassOf 'cardiogenetic disease' 'cardiac conduction disease with or without cardiomyoopathy' SubClassOf 'cardiac rhythm disease' http://purl.obolibrary.org/obo/MONDO_0980712 dyschromatosis, ichthyosis, deafness, and atopic disease 'dyschromatosis, ichthyosis, deafness, and atopic disease' SubClassOf 'hereditary disease' 'dyschromatosis, ichthyosis, deafness, and atopic disease' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0980711 brain small vessel disease 6 with leukoencephalopathy 'brain small vessel disease 6 with leukoencephalopathy' SubClassOf 'familial porencephaly' http://purl.obolibrary.org/obo/MONDO_0980710 neurodevelopmental disorder with structural brain abnormalities and craniofacial abnormalities 'neurodevelopmental disorder with structural brain abnormalities and craniofacial abnormalities' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980729 immunodeficiency 134 (Epstein-Barr virus-specific) 'immunodeficiency 134 (Epstein-Barr virus-specific)' SubClassOf 'immunodeficiency disease' http://purl.obolibrary.org/obo/MONDO_0980728 developmental delay with sleep apnea 'developmental delay with sleep apnea' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0980727 developmental delay with variable cardiac and renal congenital anomalies and dysmorphic facies 'developmental delay with variable cardiac and renal congenital anomalies and dysmorphic facies' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0980726 Ververi-Brady syndrome 2 'Ververi-Brady syndrome 2' SubClassOf 'Ververi-Brady syndrome' http://purl.obolibrary.org/obo/MONDO_0980725 fetomaternal alloimmune thrombocytopenia 3 'fetomaternal alloimmune thrombocytopenia 3' SubClassOf 'fetal and neonatal alloimmune thrombocytopenia' http://purl.obolibrary.org/obo/MONDO_0980724 fetomaternal alloimmune thrombocytopenia 2 'fetomaternal alloimmune thrombocytopenia 2' SubClassOf 'fetal and neonatal alloimmune thrombocytopenia' http://purl.obolibrary.org/obo/MONDO_0980723 fetomaternal alloimmune thrombocytopenia 1 'fetomaternal alloimmune thrombocytopenia 1' SubClassOf 'fetal and neonatal alloimmune thrombocytopenia' http://purl.obolibrary.org/obo/MONDO_0980722 Stargardt disease 5 'Stargardt disease 5' SubClassOf 'Stargardt disease' http://purl.obolibrary.org/obo/MONDO_0980721 rhabdomyolysis, susceptibility to, 2 'rhabdomyolysis, susceptibility to, 2' SubClassOf 'rhabdomyolysis, susceptibility to' http://purl.obolibrary.org/obo/MONDO_0980708 spermatogenic failure 102 'spermatogenic failure 102' SubClassOf 'spermatogenic failure' http://purl.obolibrary.org/obo/MONDO_0980707 Valence-Farazi cerebellar ataxia syndrome 'Valence-Farazi cerebellar ataxia syndrome' SubClassOf 'syndromic disease' 'Valence-Farazi cerebellar ataxia syndrome' SubClassOf 'nervous system disorder' http://purl.obolibrary.org/obo/MONDO_0980706 neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia 'neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980705 congenital disorder of glycosylation, type IIcc 'congenital disorder of glycosylation, type IIcc' SubClassOf 'congenital disorder of glycosylation type II' http://purl.obolibrary.org/obo/MONDO_0980704 neurocardiorenal malformation syndrome 'neurocardiorenal malformation syndrome' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980703 Harel-Tora neurodevelopmental syndrome 'Harel-Tora neurodevelopmental syndrome' SubClassOf 'syndromic disease' 'Harel-Tora neurodevelopmental syndrome' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980702 immune dysregulation, neurodevelopmental defects, and colitis 'immune dysregulation, neurodevelopmental defects, and colitis' SubClassOf 'hereditary disease' 'immune dysregulation, neurodevelopmental defects, and colitis' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0980701 sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2 'sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2' SubClassOf 'sulfite oxidase deficiency due to molybdenum cofactor deficiency' http://purl.obolibrary.org/obo/MONDO_0980709 neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities 'neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980700 neurodevelopmental disorder with speech delay and behavioral abnormalities 'neurodevelopmental disorder with speech delay and behavioral abnormalities' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0980699 neurodevelopmental disorder with growth impairment, quadriparesis, and poor or absent speech 'neurodevelopmental disorder with growth impairment, quadriparesis, and poor or absent speech' SubClassOf 'neurodevelopmental disorder' http://purl.obolibrary.org/obo/MONDO_0979881 infection-induced acute-onset axonal neuropathy 'infection-induced acute-onset axonal neuropathy' SubClassOf 'nervous system disorder' 'infection-induced acute-onset axonal neuropathy' SubClassOf 'post-infectious disorder' http://purl.obolibrary.org/obo/MONDO_0980759 follicular lymphoma, susceptibility to 'follicular lymphoma, susceptibility to' SubClassOf 'hereditary neoplastic syndrome' http://purl.obolibrary.org/obo/MONDO_0980757 periodontitis, aggressive 'periodontitis, aggressive' SubClassOf 'chronic periodontitis' 'periodontitis, aggressive' SubClassOf 'hereditary disease' http://purl.obolibrary.org/obo/MONDO_0980756 congenital myopathy 28 with rigid spine 'congenital myopathy 28 with rigid spine' SubClassOf 'congenital myopathy' http://purl.obolibrary.org/obo/MONDO_0980755 mitochondrial complex IV deficiency, nuclear type 24 'mitochondrial complex IV deficiency, nuclear type 24' SubClassOf 'mitochondrial complex IV deficiency, nuclear-type' http://purl.obolibrary.org/obo/MONDO_0980752 leukoencephalopathy without lacunae, adult-onset 'leukoencephalopathy without lacunae, adult-onset' SubClassOf 'leukodystrophy' http://purl.obolibrary.org/obo/MONDO_0980751 Ramond-Elliott neurodevelopmental syndrome 'Ramond-Elliott neurodevelopmental syndrome' SubClassOf 'neurodevelopmental disorder' 'Ramond-Elliott neurodevelopmental syndrome' SubClassOf 'syndromic disease' http://purl.obolibrary.org/obo/MONDO_0980764 scoliosis, isolated, susceptibility to 'scoliosis, isolated, susceptibility to' SubClassOf 'inherited disease susceptibility' http://purl.obolibrary.org/obo/MONDO_0980763 dental radicular dysplasia 'dental radicular dysplasia' SubClassOf 'tooth disorder' 'dental radicular dysplasia' SubClassOf 'hereditary disease'