primary myelofibrosis https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/myelofibrosis Agnogenic myeloid metaplasia MONDO:0009692 myelofibrosis with myeloid metaplasia, somatic CIMF myeloid metaplasia AMM myelosclerosis with myeloid metaplasia idiopathic bone marrow fibrosis ONCOTREE:PMF Myelofibrosis with myeloid metaplasia is a myeloproliferative disease with annual incidence of approximately 1 case per 100,000 individuals and age at diagnosis around 60 (an increased prevalence is noted in Ashkenazi Jews). Clinical manifestations depend on the type of blood cell affected and may include anemia, pallor, splenomegaly, hypermetabolic state, petechiae, ecchymosis, bleeding, lymphadenopathy, hepatomegaly, portal hypertension. myelofibrosis, somatic idiopathic myelofibrosis icd11.foundation:336704235 ICD9:289.83 MESH:D055728 primary myelofibrosis OMIM:254450 chronic idiopathic myelofibrosis osteomyelofibrosis DOID:4971 NORD:1611 EFO:0002430 GARD:0008618 ICD10CM:D47.4 UMLS:C0001815 NCIT:C2862 ICDO:9961/3 icd11.foundation:1407285327 ICD9:238.76 MEDGEN:7929 Orphanet:824 myelofibrosis with myeloid metaplasia acquired aplastic anemia myeloproliferative neoplasm