{"orpha":97992,"name":"Rare hematologic disease","type":"Category","group":"Group of disorders","status":"active","flags":["Head of classification"],"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-97992/","orphanet_url":"https://www.orpha.net/en/disease/detail/97992","names":{"fr":{"name":"Maladie hématologique rare"},"de":{"name":"Hämatologische Krankheit, seltene"},"es":{"name":"Enfermedad hematológica rara"},"it":{"name":"Malattia ematologica rara"},"nl":{"name":"Zeldzame hematologische ziekte"},"pt":{"name":"Doença hematológica rara"},"pl":{"name":"Rzadkie choroby hematologiczne"},"cs":{"name":"Vzácná hematologická onemocnění"},"uk":{"name":"Рідкісне гематологічне захворювання"},"zh":{"name":"罕见血液系统疾病"},"tr":{"name":"Nadir hematolojik hastalık"}},"xrefs":[{"source":"MONDO","code":"5570","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681542","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[{"orpha":86816,"name":"Congenital analbuminemia","type":"Disease"},{"orpha":98427,"name":"Erythrocytosis","type":"Clinical group"},{"orpha":619233,"name":"Hereditary persistence of fetal hemoglobin-intellectual disability syndrome","type":"Disease"},{"orpha":440731,"name":"L-ferritin deficiency","type":"Biological anomaly"},{"orpha":707993,"name":"Methemoglobinemia-related cyanosis","type":"Category"},{"orpha":450322,"name":"Polyclonal hyperviscosity syndrome","type":"Clinical syndrome"},{"orpha":108997,"name":"Rare anemia","type":"Category"},{"orpha":98429,"name":"Rare coagulation disorder","type":"Category"},{"orpha":570470,"name":"Ricin poisoning","type":"Disease"},{"orpha":91139,"name":"Simple cryoglobulinemia","type":"Disease"},{"orpha":68347,"name":"Tumor of hematopoietic and lymphoid tissues","type":"Category"},{"orpha":617294,"name":"Twin anemia-polycythemia sequence","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}