{"orpha":98364,"name":"Rare constitutional hemolytic anemia due to a red cell membrane anomaly","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-98364/","orphanet_url":"https://www.orpha.net/en/disease/detail/98364","names":{"fr":{"name":"Anémie hémolytique constitutionnelle rare par anomalie de la membrane du globule rouge"},"de":{"name":"Seltene konstitutionelle hämolytische Anämie durch Membrananomalie der roten Blutkörperchen"},"es":{"name":"Anemia hemolítica constitucional rara por una anomalía de la membrana eritrocitaria"},"it":{"name":"Anemia emolitica costituzionale rara da anomalie della membrana dei globuli rossi"},"nl":{"name":"Zeldzame constitutionele hemolytische anemie als gevolg van een rode celmembraananomalie"},"pt":{"name":"Anemia por anomalia da membrana dos glóbulos vermelhos"},"pl":{"name":"Rzadka niedokrwistość hemolityczna konstytucjonalna z powodu anomalii błony komórkowej czerwonych krwinek"},"cs":{"name":"Vzácné konstituční hemolytické anémie způsobené anomáliemi membrány červených krvinek"},"uk":{"name":"Рідкісна конституціональна гемолітична анемія через аномалію еритроцитарної мембрани"},"zh":{"name":"红细胞膜异常所致罕见原发性溶血性贫血"},"tr":{"name":"Kırmızı hücre zarı anomalisine bağlı nadir yapısal hemolitik anemi"}},"xrefs":[{"source":"UMLS","code":"C5681716","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":182043,"name":"Rare constitutional hemolytic anemia","classifications":[156,194]}],"children":[{"orpha":98366,"name":"Constitutional hemolytic anemia due to acanthocytosis","type":"Category"},{"orpha":93610,"name":"Distal renal tubular acidosis with anemia","type":"Clinical subtype"},{"orpha":288,"name":"Hereditary elliptocytosis","type":"Disease"},{"orpha":822,"name":"Hereditary spherocytosis","type":"Disease"},{"orpha":98365,"name":"Hereditary stomatocytosis","type":"Clinical group"},{"orpha":169464,"name":"Primary CD59 deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}