{"orpha":98867,"name":"Hereditary pyropoikilocytosis","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Hereditary elliptocytosis","url":"https://raremap.alftech.space/d/ORPHA-98867/","orphanet_url":"https://www.orpha.net/en/disease/detail/98867","names":{"fr":{"name":"Pyropoïkilocytose héréditaire"},"de":{"name":"Pyropoikilozytose, hereditäre"},"es":{"name":"Piropoiquilocitosis hereditaria"},"it":{"name":"Piropoichilocitosi ereditaria"},"nl":{"name":"Hereditaire pyropoikilocytose","synonyms":["Erfelijke pyropoikilocytose"]},"pt":{"name":"Piropoiquilocitose hereditária"},"pl":{"name":"Piropoikilocytoza dziedziczna"},"cs":{"name":"Hereditární pyropoikilocytóza"},"uk":{"name":"Спадковий піропойкілоцитоз"},"zh":{"name":"遗传性热变性异形红细胞增多症"},"tr":{"name":"Kalıtsal piropoikilositoz"}},"xrefs":[{"source":"OMIM","code":"266140","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0520739","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":288,"name":"Hereditary elliptocytosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}