{"orpha":158300,"name":"Rare genetic hematologic disease","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-158300/","orphanet_url":"https://www.orpha.net/en/disease/detail/158300","names":{"fr":{"name":"Maladie hématologique génétique rare"},"de":{"name":"Hämatologische Krankheit, genetisch bedingte"},"es":{"name":"Enfermedades hematológicas genéticas raras"},"it":{"name":"Malattia ematologica genetica"},"nl":{"name":"Zeldzame genetische hematologische ziekte"},"pt":{"name":"Doença hematológica genética"},"pl":{"name":"Rzadka genetyczna choroba hematologiczna"},"cs":{"name":"Vzácná dědičná onemocnění krvetvorby"},"uk":{"name":"Рідкісне генетично обумовлене гематологічне захворювання"},"zh":{"name":"罕见遗传性血液病"},"tr":{"name":"Nadir görülen genetik hematolojik hastalık"}},"xrefs":[{"source":"MONDO","code":"15549","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680681","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":621,"name":"Autosomal recessive methemoglobinemia","type":"Disease"},{"orpha":86816,"name":"Congenital analbuminemia","type":"Disease"},{"orpha":250165,"name":"Genetic polycythemia","type":"Category"},{"orpha":330041,"name":"Hemoglobin M disease","type":"Disease"},{"orpha":619233,"name":"Hereditary persistence of fetal hemoglobin-intellectual disability syndrome","type":"Disease"},{"orpha":440731,"name":"L-ferritin deficiency","type":"Biological anomaly"},{"orpha":447,"name":"Paroxysmal nocturnal hemoglobinuria","type":"Disease"},{"orpha":183651,"name":"Rare constitutional anemia","type":"Category"},{"orpha":183654,"name":"Rare genetic coagulation disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}