{"orpha":79360,"name":"Other genetic epidermal disease","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-79360/","orphanet_url":"https://www.orpha.net/en/disease/detail/79360","names":{"fr":{"name":"Autre maladie génétique de l'épiderme"},"de":{"name":"Hautkrankheit, genetische, unklassifizierte"},"es":{"name":"Enfermedad epidérmica génetica sin clasificar"},"it":{"name":"Malattie genetice dell'epidermide non classificate"},"nl":{"name":"Genetische niet-geclasificeerde epidermale ziekte"},"pt":{"name":"Doença epidérmica, sindrómica"},"pl":{"name":"Genetyczne niesklasyfikowane zaburzenia naskórka"},"cs":{"name":"Jiné geneticky podmíněné postižení epidermis"},"uk":{"name":"Інші генетичні епідермальні захворювання"},"zh":{"name":"其他遗传性表皮疾病"},"tr":{"name":"Diğer genetik epidermal hastalık"}},"xrefs":[{"source":"MONDO","code":"19275","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681490","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":183426,"name":"Genetic epidermal disorder","classifications":[156]}],"children":[{"orpha":1658,"name":"Absence of fingerprints-congenital milia syndrome","type":"Disease"},{"orpha":90301,"name":"Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome","type":"Disease"},{"orpha":163931,"name":"Acrodermatitis continua of Hallopeau","type":"Disease"},{"orpha":2388,"name":"Choreoacanthocytosis","type":"Disease"},{"orpha":218,"name":"Darier disease","type":"Disease"},{"orpha":247353,"name":"Generalized pustular psoriasis","type":"Disease"},{"orpha":1867,"name":"Hereditary bullous dystrophy, macular type","type":"Disease"},{"orpha":409,"name":"Hyperkeratosis lenticularis perstans","type":"Disease"},{"orpha":50943,"name":"Keratolytic winter erythema","type":"Disease"},{"orpha":2339,"name":"Keratosis follicularis-dwarfism-cerebral atrophy syndrome","type":"Malformation syndrome"},{"orpha":498,"name":"Keratosis pilaris atrophicans","type":"Clinical group"},{"orpha":158687,"name":"Lethal acantholytic erosive disorder","type":"Disease"},{"orpha":294023,"name":"Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome","type":"Disease"},{"orpha":163927,"name":"Pustulosis palmaris et plantaris","type":"Disease"},{"orpha":85165,"name":"Severe achondroplasia-developmental delay-acanthosis nigricans syndrome","type":"Disease"},{"orpha":369992,"name":"Severe dermatitis-multiple allergies-metabolic wasting syndrome","type":"Disease"},{"orpha":482606,"name":"X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}