{"orpha":281210,"name":"X-linked ichthyosis syndrome","type":"Clinical group","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-281210/","orphanet_url":"https://www.orpha.net/en/disease/detail/281210","names":{"fr":{"name":"Ichtyose syndromique liée à l'X"},"de":{"name":"Ichthyose-Syndrom, X-chromosomales"},"es":{"name":"Síndrome de ictiosis ligada al cromosoma X"},"it":{"name":"Ittiosi sindromica legata all'X"},"nl":{"name":"X-gebonden ichthyosis-syndroom"},"pt":{"name":"Síndrome ictiose ligada ao X"},"pl":{"name":"Zespół rybiej łuski sprzężony z chromosomem X"},"cs":{"name":"X-vázané syndromy s ichtyózou"},"uk":{"name":"Х-зчеплений синдром іхтіозу"},"zh":{"name":"X连锁遗传鱼鳞病综合征"},"tr":{"name":"X'e bağlı iktiyoz sendromu"}},"xrefs":[{"source":"ICD-10","code":"Q80.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"LD27.2","qualifier":"NTBT","icd_relation":"specific","validated":true,"icd11_uri":"53659080"},{"source":"MONDO","code":"0017269","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17269","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0079588","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10048063","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":281085,"name":"Inherited ichthyosis syndromic form","classifications":[156,187]}],"children":[{"orpha":139,"name":"CHILD syndrome","type":"Disease"},{"orpha":2273,"name":"Ichthyosis follicularis-alopecia-photophobia syndrome","type":"Disease"},{"orpha":281090,"name":"Syndromic recessive X-linked ichthyosis","type":"Disease"},{"orpha":35173,"name":"X-linked dominant chondrodysplasia punctata","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable","X-linked dominant","X-linked recessive"],"onset":[],"prevalence":[],"phenotypes":null}