{"orpha":98366,"name":"Constitutional hemolytic anemia due to acanthocytosis","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Constitutional hemolytic anemia due to acanthocytic disorder"],"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-98366/","orphanet_url":"https://www.orpha.net/en/disease/detail/98366","names":{"fr":{"name":"Anémie hémolytique constitutionnelle due à une acanthocytose","synonyms":["Anémie hémolytique constitutionnelle due à une maladie acanthocytique"]},"de":{"name":"Konstitutionelle hämolytische Anämie durch Akanthozytose"},"es":{"name":"Anemia hemolítica constitucional por acantocitosis","synonyms":["Anemia hemolítica constitucional por trastorno acantocítico"]},"it":{"name":"Anemia emolitica costituzionale da acantocitosi","synonyms":["Anemia emolitica costituzionale da malattia acantocitica"]},"nl":{"name":"Constitutionele hemolytische anemie als gevolg van acanthocytose","synonyms":["Constitutionele hemolytische anemie als gevolg van een acanthocytische stoornis"]},"pt":{"name":"Acantocitose"},"pl":{"name":"Niedokrwistość hemolityczna konstytucjonalna z powodu akantolizy","synonyms":["Dziedzina anemia hemolityczna z powodu akantocytozy"]},"cs":{"name":"Konstituční hemolytická anémie způsobená akantocytózou","synonyms":["Constitutional hemolytic anemia due to acanthocytic disorder"]},"uk":{"name":"Конституціональна гемолітична анемія внаслідок акантоцитозу","synonyms":["Конституційна гемолітична анемія внаслідок акантоцитарної недостатності"]},"zh":{"name":"棘红细胞增多症所致先天性溶血性贫血","synonyms":["棘红细胞增多病所致先天性溶血性贫血"]},"tr":{"name":"Akantositoza bağlı yapısal hemolitik anemi","synonyms":["Akantositik bozukluğa bağlı yapısal hemolitik anemi"]}},"xrefs":[{"source":"ICD-11","code":"3A10.Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1270003217"},{"source":"UMLS","code":"C0687751","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":98364,"name":"Rare constitutional hemolytic anemia due to a red cell membrane anomaly","classifications":[156,194]}],"children":[{"orpha":14,"name":"Abetalipoproteinemia","type":"Disease"},{"orpha":59306,"name":"McLeod neuroacanthocytosis syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}