{"orpha":98865,"name":"Homozygous 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-98865/","orphanet_url":"https://www.orpha.net/en/disease/detail/98865","names":{"fr":{"name":"Elliptocytose héréditaire homozygote"},"de":{"name":"Elliptozytose, hereditäre, homozygote"},"es":{"name":"Eliptocitosis hereditaria homocigota"},"it":{"name":"Ellissocitosi ereditaria omozigote"},"nl":{"name":"Homozygote erfelijke elliptocytose"},"pt":{"name":"Eliptocitose hereditária homozigótica"},"pl":{"name":"Homozygotyczna dziedziczna eliptocytoza"},"cs":{"name":"Homozygotní hereditární eliptocytóza"},"uk":{"name":"Гомозиготний спадковий еліптоцитоз"},"zh":{"name":"纯合型遗传性椭圆形红细胞增多症"},"tr":{"name":"Homozigot 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}