{"orpha":222628,"name":"Hereditary poikiloderma","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-222628/","orphanet_url":"https://www.orpha.net/en/disease/detail/222628","names":{"fr":{"name":"Poïkilodermie héréditaire"},"de":{"name":"Poikilodermie, hereditäre"},"es":{"name":"Poiquilodermia hereditaria"},"it":{"name":"Poichilodermia ereditaria"},"nl":{"name":"Erfelijke poikilodermie"},"pt":{"name":"Poiquilodermia hereditária"},"pl":{"name":"Poikilodermia dziedziczna"},"cs":{"name":"Hereditární poikilodermie"},"uk":{"name":"Спадкова пойкилодермія"},"zh":{"name":"遗传性皮肤异色病"},"tr":{"name":"Kalıtsal poikiloderma"}},"xrefs":[{"source":"MONDO","code":"0016382","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16382","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680891","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":306539,"name":"OBSOLETE: Hereditary acrokeratotic poikiloderma of Kindler-Weary","status":"inactive"}],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":79353,"name":"Epidermal disease","classifications":[187]},{"orpha":183426,"name":"Genetic epidermal disorder","classifications":[156]}],"children":[{"orpha":1775,"name":"Dyskeratosis congenita","type":"Disease"},{"orpha":2907,"name":"Hereditary acrokeratotic poikiloderma","type":"Disease"},{"orpha":221043,"name":"Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome","type":"Disease"},{"orpha":221039,"name":"Hereditary sclerosing poikiloderma, Weary type","type":"Disease"},{"orpha":221046,"name":"Poikiloderma with neutropenia","type":"Disease"},{"orpha":2909,"name":"Rothmund-Thomson syndrome","type":"Disease"},{"orpha":902,"name":"Werner syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}