{"orpha":79363,"name":"Hair anomaly","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-79363/","orphanet_url":"https://www.orpha.net/en/disease/detail/79363","names":{"fr":{"name":"Anomalie des cheveux"},"de":{"name":"Haaranomalie"},"es":{"name":"Anomalía del cabello"},"it":{"name":"Anomalie dei capelli"},"nl":{"name":"Haaranomalie"},"pt":{"name":"Anomalia do cabelo"},"pl":{"name":"Anomalie włosów"},"cs":{"name":"Anomálie vlasů"},"uk":{"name":"Аномалія волосся"},"zh":{"name":"毛发异常"},"tr":{"name":"Saç anomalisi"}},"xrefs":[{"source":"MONDO","code":"0019278","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19278","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0265991","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":79362,"name":"Epidermal appendage anomaly","classifications":[187]}],"children":[{"orpha":79364,"name":"Alopecia","type":"Category"},{"orpha":411788,"name":"Familial isolated trichomegaly","type":"Disease"},{"orpha":79366,"name":"Isolated hair shaft abnormality","type":"Category"},{"orpha":79365,"name":"Rare disorder with hypertrichosis","type":"Category"},{"orpha":79367,"name":"Syndromic hair shaft abnormality","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}