{"orpha":281082,"name":"Inherited non-syndromic ichthyosis","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-281082/","orphanet_url":"https://www.orpha.net/en/disease/detail/281082","names":{"fr":{"name":"Ichtyose héréditaire non syndromique"},"de":{"name":"Ichthyose, hereditäre, nicht-syndromale Form"},"es":{"name":"Ictiosis hereditaria no sindrómica"},"it":{"name":"Ittiosi ereditaria, forma non sindromica"},"nl":{"name":"Overgeërfde ichthyosis niet-syndromale vorm"},"pt":{"name":"Ictiose hereditária forma não-sindromática"},"pl":{"name":"Dziedziczna rybia łuska postać niesyndromiczna"},"cs":{"name":"Dědičné nesyndromické ichtyózy"},"uk":{"name":"Спадковий несиндромальний іхтіоз"},"zh":{"name":"遗传性非综合征型鱼鳞病"},"tr":{"name":"Kalıtsal sendromik-olmayan iktiyoz"}},"xrefs":[{"source":"ICD-11","code":"EC20.0","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"213831678"},{"source":"MONDO","code":"17262","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681020","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":183435,"name":"Inherited ichthyosis","classifications":[156,187]}],"children":[{"orpha":281097,"name":"Autosomal recessive congenital ichthyosis","type":"Clinical group"},{"orpha":317,"name":"Erythrokeratodermia variabilis","type":"Disease"},{"orpha":281103,"name":"Keratinopathic ichthyosis","type":"Clinical group"},{"orpha":79395,"name":"Keratoderma hereditarium mutilans with ichthyosis","type":"Disease"},{"orpha":281201,"name":"Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome","type":"Disease"},{"orpha":817,"name":"Peeling skin syndrome","type":"Clinical group"},{"orpha":444138,"name":"Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome","type":"Disease"},{"orpha":461,"name":"Recessive X-linked ichthyosis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Point prevalence","qualification":"Value and class","class":"1-9 / 100 000","value":1.13,"area":"France","status":"Not yet validated","source":"24393603[PMID]"}],"phenotypes":null}