{"orpha":182047,"name":"Rare acquired hemolytic anemia","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-182047/","orphanet_url":"https://www.orpha.net/en/disease/detail/182047","names":{"fr":{"name":"Anémie hémolytique acquise rare"},"de":{"name":"Hämolytische Anämie, erworbene, seltene"},"es":{"name":"Anemia hemolítica adquirida rara"},"it":{"name":"Anemia emolitica acquisita rara"},"nl":{"name":"Zeldzame verworven hemolytische anemie"},"pt":{"name":"Anemia hemolítica adquirida rara"},"pl":{"name":"Rzadka nabyta niedokrwistość hemolityczna"},"cs":{"name":"Vzácné získané hemolytické anémie"},"uk":{"name":"Рідкісна набута гемолітична анемія"},"zh":{"name":"罕见获得性溶血性贫血"},"tr":{"name":"Nadir edinsel hemolitik anemi"}},"xrefs":[{"source":"MONDO","code":"15911","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680604","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":98363,"name":"Rare hemolytic anemia","classifications":[194]}],"children":[{"orpha":98375,"name":"Autoimmune hemolytic anemia","type":"Clinical group"},{"orpha":275938,"name":"Hemolytic disease due to fetomaternal alloimmunization","type":"Category"},{"orpha":544482,"name":"Infection-related hemolytic uremic syndrome","type":"Disease"},{"orpha":447,"name":"Paroxysmal nocturnal hemoglobinuria","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}