{"code":"C75003","name":"Synpolydactyly","terminology":"ncit","version":"26.10d","conceptStatus":"DEFAULT","leaf":false,"active":true,"synonyms":[{"name":"Synpolydactyly","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Synpolydactyly","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"A rare genetic disorder characterized by malformations in the hands and feet.  The abnormalities include increased number of fingers and toes and fusion of digits into one large digit.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P366","type":"Legacy Concept Name","value":"Synpolydactyly"},{"code":"P106","type":"Semantic_Type","value":"Disease or Syndrome"},{"code":"P207","type":"UMLS_CUI","value":"C2699746"}],"parents":[{"code":"C53543","name":"Rare Non-Neoplastic Disorder"},{"code":"C28193","name":"Syndrome"}],"roles":[{"code":"R108","type":"Disease_Has_Finding","relatedCode":"C42094","relatedName":"Rare Lesion"}]}