{"orpha":183484,"name":"Genetic subcutaneous tissue disorder","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-183484/","orphanet_url":"https://www.orpha.net/en/disease/detail/183484","names":{"fr":{"name":"Maladie génétique du tissu sous-cutané"},"de":{"name":"Gewebekrankheit, subkutane, genetisch bedingte"},"es":{"name":"Enfermedad genética del tejido subcutáneo"},"it":{"name":"Malattia genetica del tessuto sottocutaneo"},"nl":{"name":"Genetische aandoening van subcutaan weefsel","synonyms":["Genetische aandoening van onderhuids weefsel"]},"pt":{"name":"Doença genética do tecido subcutâneo"},"pl":{"name":"Genetic subcutaneous tissue disorder"},"cs":{"name":"Geneticky podmíněná onemocnění podkožní tkáně","synonyms":["Geneticky podmíněná onemocnění podkožních tkání"]},"uk":{"name":"Генетично обумовлене захворювання підшкірної клітковини"},"zh":{"name":"遗传性皮下组织异常"},"tr":{"name":"Genetik deri altı doku bozukluğu"}},"xrefs":[{"source":"MONDO","code":"15949","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680570","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":68346,"name":"Rare genetic skin disease","classifications":[156]}],"children":[{"orpha":404454,"name":"Alacrimia-choreoathetosis-liver dysfunction syndrome","type":"Disease"},{"orpha":140944,"name":"CLOVES syndrome","type":"Malformation syndrome"},{"orpha":909,"name":"Cerebrotendinous xanthomatosis","type":"Disease"},{"orpha":2396,"name":"Encephalocraniocutaneous lipomatosis","type":"Disease"},{"orpha":199279,"name":"Familial angiolipomatosis","type":"Disease"},{"orpha":199276,"name":"Familial multiple lipomatosis","type":"Disease"},{"orpha":333,"name":"Farber disease","type":"Disease"},{"orpha":337,"name":"Fibrodysplasia ossificans progressiva","type":"Disease"},{"orpha":98305,"name":"Genetic lipodystrophy","type":"Category"},{"orpha":468666,"name":"Isolated generalized anhidrosis with normal sweat glands","type":"Disease"},{"orpha":2398,"name":"Multiple symmetric lipomatosis","type":"Disease"},{"orpha":529,"name":"Roch-Leri mesosomatous lipomatosis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}