{"orpha":566857,"name":"Aprosencephaly","type":"Clinical subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This disease is described under Aprosencephaly/atelencephaly spectrum","url":"https://raremap.alftech.space/d/ORPHA-566857/","orphanet_url":"https://www.orpha.net/en/disease/detail/566857","names":{"fr":{"name":"Aprosencéphalie"},"de":{"name":"Aprosenzephalie"},"es":{"name":"Aprosencefalia"},"it":{"name":"Aprosencefalia"},"nl":{"name":"Aprosencefalie"},"pt":{"name":"Aprosencefalia"},"pl":{"name":"Aprosencefalia"},"cs":{"name":"Aprosencefalie"},"uk":{"name":"Апросенцефалія"},"zh":{"name":"脑前部缺无"},"tr":{"name":"Aprosensefali"}},"xrefs":[{"source":"ICD-10","code":"Q04.3","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LA05.Y","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"MONDO","code":"0035450","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0431349","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":566847,"name":"Aprosencephaly/atelencephaly spectrum","classifications":[147,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":[],"prevalence":[],"phenotypes":null}