{"orpha":68383,"name":"Rare constitutional aplastic 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-68383/","orphanet_url":"https://www.orpha.net/en/disease/detail/68383","names":{"fr":{"name":"Aplasie médullaire constitutionnelle rare"},"de":{"name":"Aplastische Anämie, konstitutionelle seltene"},"es":{"name":"Anemia aplásica constitucional rara"},"it":{"name":"Anemia aplastica costituzionale rara"},"nl":{"name":"Zeldzame constitutionele aplastische anemie"},"pt":{"name":"Anemia aplásica constitucional rara"},"pl":{"name":"Rzadka aplazja szpiku"},"cs":{"name":"Vzácná konstituční aplastická anémie"},"uk":{"name":"Рідкісна конституційна апластична анемія"},"zh":{"name":"罕见造血组分相关再生障碍性贫血"},"tr":{"name":"Nadir yapısal aplastik anemi"}},"xrefs":[{"source":"ICD-10","code":"D61.0","qualifier":"NTBT","icd_relation":"specific","validated":true},{"source":"MONDO","code":"1713","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681331","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":182040,"name":"Rare aplastic anemia","classifications":[194,233]},{"orpha":183651,"name":"Rare constitutional anemia","classifications":[156]}],"children":[{"orpha":611216,"name":"Aplastic anemia-intellectual disability-dwarfism syndrome","type":"Disease"},{"orpha":314399,"name":"Autosomal dominant aplasia and myelodysplasia","type":"Disease"},{"orpha":725898,"name":"Bone marrow failure-diabetes mellitus syndrome","type":"Disease"},{"orpha":3319,"name":"Congenital amegakaryocytic thrombocytopenia","type":"Disease"},{"orpha":124,"name":"Diamond-Blackfan anemia","type":"Disease"},{"orpha":1775,"name":"Dyskeratosis congenita","type":"Disease"},{"orpha":84,"name":"Fanconi anemia","type":"Malformation syndrome"},{"orpha":3322,"name":"Hoyeraal-Hreidarsson syndrome","type":"Disease"},{"orpha":401764,"name":"Pancytopenia-developmental delay syndrome","type":"Disease"},{"orpha":726036,"name":"Red cell aplasia-microcephaly-seizure-developmental delay syndrome","type":"Disease"},{"orpha":3088,"name":"Revesz syndrome","type":"Malformation syndrome"},{"orpha":811,"name":"Shwachman-Diamond syndrome","type":"Disease"},{"orpha":3466,"name":"WT limb-blood syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}