{"orpha":183460,"name":"Genetic 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-183460/","orphanet_url":"https://www.orpha.net/en/disease/detail/183460","names":{"fr":{"name":"Anomalie génétique des glandes sébacées"},"de":{"name":"Talgdrüsenanomalie, genetisch bedingte"},"es":{"name":"Anomalía genética de las glándulas sebáceas"},"it":{"name":"Anomalia delle ghiandole sebacee di origine genetica"},"nl":{"name":"Genetische vetklieranomalie"},"pt":{"name":"Anomalia genética das glândulas sebáceas"},"pl":{"name":"Wada gruczołów łojowych uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné anomálie mazových žláz"},"uk":{"name":"Генетично обумовлена аномалія сальних залоз"},"zh":{"name":"遗传性皮脂腺遗传异常"},"tr":{"name":"Genetik yağ bezi anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5680577","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":183447,"name":"Genetic epidermal appendage anomaly","classifications":[156]}],"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}