{"orpha":182043,"name":"Rare constitutional 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-182043/","orphanet_url":"https://www.orpha.net/en/disease/detail/182043","names":{"fr":{"name":"Anémie hémolytique constitutionnelle rare"},"de":{"name":"Hämolytische Anämie, konstitutionelle, seltene"},"es":{"name":"Anemia hemolítica constitucional rara"},"it":{"name":"Anemia emolitica costituzionale rara"},"nl":{"name":"Zeldzame constitutionele hemolytische anemie"},"pt":{"name":"Anemia hemolítica constitucional rara"},"pl":{"name":"Rzadka konstytucjonalna niedokrwistość hemolityczna"},"cs":{"name":"Vzácné konstituční hemolytické anémie"},"uk":{"name":"Рідкісна конституціональна гемолітична анемія"},"zh":{"name":"罕见全身性溶血性贫血"},"tr":{"name":"Nadir yapısal hemolitik anemi"}},"xrefs":[{"source":"MONDO","code":"15910","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680605","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":183651,"name":"Rare constitutional anemia","classifications":[156]},{"orpha":98363,"name":"Rare hemolytic anemia","classifications":[194]}],"children":[{"orpha":86818,"name":"Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome","type":"Disease"},{"orpha":727394,"name":"Autosomal recessive KLF1-related severe anemia","type":"Disease"},{"orpha":79293,"name":"Familial LCAT deficiency","type":"Clinical subtype"},{"orpha":576742,"name":"Genetic hemolytic uremic syndrome","type":"Category"},{"orpha":1046,"name":"Lethal hemolytic anemia-genital anomalies syndrome","type":"Malformation syndrome"},{"orpha":688581,"name":"Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome","type":"Malformation syndrome"},{"orpha":98364,"name":"Rare constitutional hemolytic anemia due to a red cell membrane anomaly","type":"Category"},{"orpha":98369,"name":"Rare constitutional hemolytic anemia due to an enzyme disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}