{"orpha":79385,"name":"Unclassified genetic skin 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-79385/","orphanet_url":"https://www.orpha.net/en/disease/detail/79385","names":{"fr":{"name":"Maladie génétique non classifiée de la peau"},"de":{"name":"Hautkrankheit, genetisch bedingte, sonstige"},"es":{"name":"Enfermedad de la piel de origen genético no clasificada"},"it":{"name":"Malattia genetica della cute non classificata"},"nl":{"name":"Niet-geclassificeerde genetische aandoening van huid"},"pt":{"name":"Doença dermatológica, genética, outra"},"pl":{"name":"Niesklasyfikowany choroby skóry pochodzenia genetycznego"},"cs":{"name":"Neklasifikované geneticky podmíněné nemoci kůže"},"uk":{"name":"Некласифіковане генетично обумовлене захворювання шкіри"},"zh":{"name":"未分类的遗传性皮肤疾病"},"tr":{"name":"Sınıflandırılmamış genetik cilt bozukluğu"}},"xrefs":[{"source":"MONDO","code":"19299","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681473","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]},{"orpha":89826,"name":"Rare skin disease","classifications":[187]}],"children":[{"orpha":1954,"name":"Congenital lethal erythroderma","type":"Disease"},{"orpha":231031,"name":"Erythema palmare hereditarium","type":"Disease"},{"orpha":83628,"name":"LUMBAR syndrome","type":"Malformation syndrome"},{"orpha":2505,"name":"Multiple benign circumferential skin creases on limbs","type":"Disease"},{"orpha":2812,"name":"Parana hard skin syndrome","type":"Disease"},{"orpha":2833,"name":"Stiff skin syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}