{"orpha":79354,"name":"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-79354/","orphanet_url":"https://www.orpha.net/en/disease/detail/79354","names":{"fr":{"name":"Ichtyose"},"de":{"name":"Ichthyose"},"es":{"name":"Ictiosis"},"it":{"name":"Ittiosi"},"nl":{"name":"Ichthyosis"},"pt":{"name":"Ictiose"},"pl":{"name":"Rybia łuska"},"cs":{"name":"Ichtyóza"},"uk":{"name":"Іхтіоз"},"zh":{"name":"鱼鳞病"},"tr":{"name":"İktiyoz"}},"xrefs":[{"source":"MONDO","code":"0019269","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19269","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D007057","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0020757","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10021198","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98296,"name":"OBSOLETE: Ichthyosis associated with a cornified cell envelope and epidermal lipid metabolism anomaly","status":"inactive"},{"type":"Referred to","orpha":98297,"name":"OBSOLETE: Ichthyosis associated with a protein catabolism anomaly","status":"inactive"},{"type":"Referred to","orpha":98298,"name":"OBSOLETE: Ichthyosis associated with a peroxisomal disease","status":"inactive"},{"type":"Referred to","orpha":98299,"name":"OBSOLETE: Ichthyosis associated with a nucleotide excision repair anomaly","status":"inactive"}],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":79353,"name":"Epidermal disease","classifications":[187]}],"children":[{"orpha":454,"name":"Acquired ichthyosis","type":"Disease"},{"orpha":183435,"name":"Inherited ichthyosis","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}