{"orpha":89826,"name":"Rare skin disease","type":"Category","group":"Group of disorders","status":"active","flags":["Head of classification"],"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-89826/","orphanet_url":"https://www.orpha.net/en/disease/detail/89826","names":{"fr":{"name":"Maladie rare de la peau"},"de":{"name":"Hautkrankheit, seltene"},"es":{"name":"Enfermedad cutánea rara"},"it":{"name":"Malattia cutanea rara"},"nl":{"name":"Zeldzame huidziekte"},"pt":{"name":"Doença de pele rara"},"pl":{"name":"Rzadkie choroby skóry"},"cs":{"name":"Vzácné kožní nemoci"},"uk":{"name":"Рідкісне шкірне захворювання"},"zh":{"name":"罕见皮肤病"},"tr":{"name":"Nadir cilt hastalığı"}},"xrefs":[{"source":"MONDO","code":"19519","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681445","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[{"orpha":315350,"name":"Autoimmune disease with skin involvement","type":"Category"},{"orpha":79377,"name":"Dermis disorder","type":"Category"},{"orpha":79362,"name":"Epidermal appendage anomaly","type":"Category"},{"orpha":79353,"name":"Epidermal disease","type":"Category"},{"orpha":79391,"name":"Immune deficiency with skin involvement","type":"Category"},{"orpha":79387,"name":"Metabolic disease with skin involvement","type":"Category"},{"orpha":90077,"name":"Other acquired skin disease","type":"Category"},{"orpha":79374,"name":"Pigmentation anomaly of the skin","type":"Category"},{"orpha":79389,"name":"Premature aging","type":"Category"},{"orpha":77240,"name":"Primary lymphedema","type":"Category"},{"orpha":79390,"name":"Rare photodermatosis","type":"Category"},{"orpha":79386,"name":"Rare skin tumor or hamartoma","type":"Category"},{"orpha":79384,"name":"Rare urticaria","type":"Category"},{"orpha":79382,"name":"Subcutaneous tissue disease","type":"Category"},{"orpha":290836,"name":"Systemic disease with skin involvement","type":"Category"},{"orpha":293815,"name":"Toxic dermatosis","type":"Category"},{"orpha":79385,"name":"Unclassified genetic skin disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}