{"orpha":171895,"name":"Myeloid hemopathy","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-171895/","orphanet_url":"https://www.orpha.net/en/disease/detail/171895","names":{"fr":{"name":"Hémopathie myéloïde"},"de":{"name":"Myeloische Hämopathie"},"es":{"name":"Hemopatía mieloide"},"it":{"name":"Emopatia mieloide"},"nl":{"name":"Myeloïde hemopathie"},"pt":{"name":"Hemopatia mielóide"},"pl":{"name":"Hemopatia szpiku"},"cs":{"name":"Myeloidní hematologická onemocnění","synonyms":["Myeleoidní hemopatie"]},"uk":{"name":"Мієлоїдна гемопатія"},"zh":{"name":"髓样血液病"},"tr":{"name":"Miyeloid hemopati"}},"xrefs":[{"source":"MONDO","code":"0015756","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15756","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680514","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":506219,"name":"Rare disorder potentially indicated for hematopoietic stem cell transplant","classifications":[233]},{"orpha":68347,"name":"Tumor of hematopoietic and lymphoid tissues","classifications":[194,202]}],"children":[{"orpha":519,"name":"Acute myeloid leukemia","type":"Clinical group"},{"orpha":52688,"name":"Myelodysplastic syndrome","type":"Clinical group"},{"orpha":98275,"name":"Myelodysplastic/myeloproliferative disease","type":"Clinical group"},{"orpha":168943,"name":"Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2","type":"Category"},{"orpha":98274,"name":"Myeloproliferative neoplasm","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}