{"orpha":477808,"name":"Other genetic dermis 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-477808/","orphanet_url":"https://www.orpha.net/en/disease/detail/477808","names":{"fr":{"name":"Autre anomalie génétique du derme"},"de":{"name":"Hautkrankheit, genetisch bedingte, sonstige"},"es":{"name":"Otros trastornos genéticos de la dermis"},"it":{"name":"Altra malattia genetica del derma"},"nl":{"name":"Andere genetische aandoening van dermis"},"pt":{"name":"Outra doença genética da derme"},"pl":{"name":"Inne genetyczne zaburzenia naskórka"},"cs":{"name":"Jiné geneticky podmíněné nemoci dermis"},"uk":{"name":"Інше генетично обумовлене захворювання дерми"},"zh":{"name":"其他遗传性皮肤病"},"tr":{"name":"Diğer genetik dermis bozukluğu"}},"xrefs":[{"source":"MONDO","code":"18798","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681256","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":183472,"name":"Genetic dermis disorder","classifications":[156]}],"children":[{"orpha":2987,"name":"Antecubital pterygium syndrome","type":"Malformation syndrome"},{"orpha":90340,"name":"Blau syndrome","type":"Disease"},{"orpha":1555,"name":"Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome","type":"Malformation syndrome"},{"orpha":79149,"name":"Dermochondrocorneal dystrophy","type":"Disease"},{"orpha":1764,"name":"Familial dysautonomia","type":"Disease"},{"orpha":353220,"name":"Familial primary localized cutaneous amyloidosis","type":"Disease"},{"orpha":468666,"name":"Isolated generalized anhidrosis with normal sweat glands","type":"Disease"},{"orpha":2028,"name":"Juvenile hyaline fibromatosis","type":"Clinical subtype"},{"orpha":140933,"name":"Linear atrophoderma of Moulin","type":"Disease"},{"orpha":530,"name":"Lipoid proteinosis","type":"Malformation syndrome"},{"orpha":2796,"name":"Pachydermoperiostosis","type":"Malformation syndrome"},{"orpha":357225,"name":"Primary non-essential cutis verticis gyrata","type":"Disease"},{"orpha":2762,"name":"Progressive osseous heteroplasia","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}