{"orpha":652510,"name":"Genetic autoinflammatory syndrome with acne and/or hidradenitis suppurativa","type":"Clinical group","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-652510/","orphanet_url":"https://www.orpha.net/en/disease/detail/652510","names":{"fr":{"name":"Syndrome génétique autoinflammatoire avec acné et/ou hidradénite suppurée"},"de":{"name":"Autoinflammatorisches Syndrom mit Akne und/oder Hidradenitis suppurativa, genetisch bedingtes"},"es":{"name":"Síndrome autoinflamatorio genético con acné y/o hidradenitis supurativa"},"it":{"name":"Sindrome genetica autoinfiammatoria con acne e/o idrosadenite suppurativa"},"nl":{"name":"Genetisch auto-inflammatoir syndroom met acne en/of hidradenitis suppurativa"},"pt":{"name":"Síndrome autoinflamatório genético com acne e/ou hidradenite supurativa"},"pl":{"name":"Genetycznie uwarunkowany zespół autozapalny z trądzikiem i/lub ropnym zapaleniem gruczołów potowych"},"cs":{"name":"Genetický autoinflamatorní syndrom s akné a/nebo hidradenitis suppurativa"},"uk":{"name":"Генетично обумовлений аутозапальний синдром з акне та/або гнійним гідраденітом"}},"xrefs":[{"source":"UMLS","code":"C5925118","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":622720,"name":"Genetic autoinflammatory syndrome with skin involvement","classifications":[156]},{"orpha":619238,"name":"Rare hereditary autoinflammatory disease","classifications":[156]}],"children":[{"orpha":69126,"name":"PAPA syndrome","type":"Disease"},{"orpha":641380,"name":"PAPASH syndrome","type":"Disease"},{"orpha":289478,"name":"PASH syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}