{"orpha":250165,"name":"Genetic polycythemia","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-250165/","orphanet_url":"https://www.orpha.net/en/disease/detail/250165","names":{"fr":{"name":"Polycythémie génétique"},"de":{"name":"Polyzythämie, genetisch bedingte"},"es":{"name":"Policitemia genética"},"it":{"name":"Policitemia genetica"},"nl":{"name":"Genetische polycytemie"},"pt":{"name":"Policitemia genética"},"pl":{"name":"Policytemia uwarunkowana genetycznie"},"cs":{"name":"Dědičné polycytémie"},"uk":{"name":"Генетично обумовлена поліцитемія"},"zh":{"name":"遗传性红细胞增多症"},"tr":{"name":"Genetik polisitemi"}},"xrefs":[{"source":"UMLS","code":"C5680689","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":158300,"name":"Rare genetic hematologic disease","classifications":[156]}],"children":[{"orpha":238536,"name":"Congenital secondary erythrocytosis","type":"Category"},{"orpha":324299,"name":"EPAS1-related polycythemia-pheochromocytoma/paraganglioma syndrome","type":"Disease"},{"orpha":90042,"name":"Primary familial and congenital erythrocytosis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}