{"orpha":98864,"name":"Common hereditary elliptocytosis","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-98864/","orphanet_url":"https://www.orpha.net/en/disease/detail/98864","names":{"fr":{"name":"Elliptocytose héréditaire commune"},"de":{"name":"Elliptozytose, stomatozytische"},"es":{"name":"Eliptocitosis común hereditaria"},"it":{"name":"Ellissocitosi ereditaria comune"},"nl":{"name":"Gewone erfelijke elliptocytose"},"pt":{"name":"Eliptocitose, comum, hereditária"},"pl":{"name":"Powszechna/Prosta dziedziczna eliptocytoza"},"cs":{"name":"Běžná hereditární eliptocytóza"},"uk":{"name":"Поширений спадковий еліптоцитоз"},"zh":{"name":"常见型遗传性椭圆形红细胞增多症"},"tr":{"name":"Yaygın kalıtsal elliptositoz"}},"xrefs":[],"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}