{"orpha":183438,"name":"Genetic erythrokeratoderma","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-183438/","orphanet_url":"https://www.orpha.net/en/disease/detail/183438","names":{"fr":{"name":"Erythrokératodermie génétique"},"de":{"name":"Erythrokeratodermie, genetisch bedingte"},"es":{"name":"Eritroqueratodermia genética"},"it":{"name":"Eritrocheratoderma genetico"},"nl":{"name":"Genetische erytrokeratodermie"},"pt":{"name":"Eritroqueratodermia genética"},"pl":{"name":"Erytrokeratodermia uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné erytrokeratodermie"},"uk":{"name":"Генетично обумовлена еритрокератодермія"},"zh":{"name":"遗传性角化性红皮病"},"tr":{"name":"Genetik eritrokeratoderma"}},"xrefs":[{"source":"UMLS","code":"C5680579","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":315,"name":"Erythrokeratoderma ''en cocardes''","type":"Disease"},{"orpha":308166,"name":"Erythrokeratoderma variabilis progressiva","type":"Clinical group"},{"orpha":476096,"name":"Erythrokeratodermia-cardiomyopathy syndrome","type":"Disease"},{"orpha":171851,"name":"MEDNIK syndrome","type":"Disease"},{"orpha":2897,"name":"Pityriasis rubra pilaris","type":"Disease"},{"orpha":1955,"name":"Spinocerebellar ataxia type 34","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}