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Transmission is autosomal dominant.","A rare genetic disease characterised by the association of unilateral or bilateral short fifth metacarpals (defined as a gap of 2 mm or more between the distal end of the fifth metacarpal bone and a tangential line connecting the distal ends of the third and fourth metacarpals), insulin resistance, and spherocytosis. Familial short stature has not been reported as part of the syndrome."],"subClassOf":["http://purl.bioontology.org/ontology/SNOMEDCT/363070008","http://purl.bioontology.org/ontology/SNOMEDCT/11164009","http://purl.bioontology.org/ontology/SNOMEDCT/897274007","http://purl.bioontology.org/ontology/SNOMEDCT/32339005","http://purl.bioontology.org/ontology/SNOMEDCT/363212003","http://purl.bioontology.org/ontology/SNOMEDCT/41443008"],"parents":[{"id":"http://purl.bioontology.org/ontology/SNOMEDCT/363070008","synonym":["Developmental hereditary disorder (disorder)"],"notation":"363070008","semanticType":["http://purl.bioontology.org/ontology/STY/T046"],"cui":["C1285243"],"prefLabel":"Developmental hereditary 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