{"orpha":295199,"name":"Synpolydactyly type 3","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":["SD2, Malik type","SD2c","SPD, Malik type","SPD3","Synpolydactyly, Malik type"],"definition":null,"note":"This disease is described under Syndactyly type 2","url":"https://raremap.alftech.space/d/ORPHA-295199/","orphanet_url":"https://www.orpha.net/en/disease/detail/295199","names":{"fr":{"name":"Sympolydactylie type 3","synonyms":["SD2 type Malik","SD2c","SPD type Malik","SPD3","Sympolydactylie type Malik"]},"de":{"name":"Synpolydaktylie Typ 3","synonyms":["SD2 Typ Malik","SD2c","SPD Typ Malik","SPD3","Synpolydaktylie, Typ Malik"]},"es":{"name":"Polisindactilia tipo 3","synonyms":["Polisindactilia tipo Malik","SD2 tipo Malik","SD2c","SPD tipo Malik","SPD3"]},"it":{"name":"Sinpolidattilia, tipo 3","synonyms":["SD2, tipo Malik","SD2c","SPD, tipo Malik","SPD3","Sinpolidattilia, tipo Malik"]},"nl":{"name":"Synpolydactylie type 3","synonyms":["SD2, Malik-type","SD2c","SPD, Malik-type","SPD3","Synpolydactylie, Malik-type"]},"pt":{"name":"Simpolidactilia, tipo 3","synonyms":["SD2, tipo Malik","SD2c","SPD, tipo Malik","SPD3","Simpolidactilia, tipo Malik"]},"pl":{"name":"Synpolidaktylia typu 3","synonyms":["SD2, typ Malika","SD2c","SPD, typ Malika","SPD3","Synpolidaktylia, typ Malika"]},"cs":{"name":"Synpolydaktylie, typ 3","synonyms":["SD2c","SPD3","SD2, Malikův typ","SPD, Malikův typ","Synpolydaktylie, Malikův typ"]},"uk":{"name":"Синполідактилія, тип 3","synonyms":["SD2, тип Малік","SD2c","SPD, тип Малік","SPD3","Синполідактилія, тип Маліка"]},"zh":{"name":"联指3型","synonyms":["并指（趾）Malik型"]},"tr":{"name":"Sinpolidaktili tip 3","synonyms":["SD2c","SPD3","SD2, Malik tipi","SPD, Malik tipi","Sinpolidaktili, Malik tipi"]}},"xrefs":[{"source":"OMIM","code":"610234","qualifier":"E","icd_relation":null,"validated":true},{"source":"ICD-10","code":"Q70.0","qualifier":"BTNT","icd_relation":"attributed","validated":true},{"source":"ICD-10","code":"Q70.2","qualifier":"BTNT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LB79.Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1671501762"},{"source":"MONDO","code":"0012447","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C565216","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1853255","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":93403,"name":"Syndactyly type 2","classifications":[147,156,199]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}