{"orpha":79372,"name":"Sebaceous gland 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-79372/","orphanet_url":"https://www.orpha.net/en/disease/detail/79372","names":{"fr":{"name":"Anomalie des glandes sébacées"},"de":{"name":"Talgdrüsenanomalie"},"es":{"name":"Anomalía de las glándulas sebáceas"},"it":{"name":"Anomalia delle ghiandole sebacee"},"nl":{"name":"Vetklieranomalie"},"pt":{"name":"Anomalia das glândulas sebáceas"},"pl":{"name":"Anomalie gruczołów łojowych"},"cs":{"name":"Anomálie mazových žlaz"},"uk":{"name":"Аномалія сальних залоз"},"zh":{"name":"皮脂腺异常"},"tr":{"name":"Sebase bez anomalisi"}},"xrefs":[{"source":"MONDO","code":"19286","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1387995","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":2750,"name":"Orofaciodigital syndrome type 1","type":"Malformation syndrome"},{"orpha":841,"name":"Sebocystomatosis","type":"Disease"},{"orpha":3184,"name":"Steatocystoma multiplex-natal teeth syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}