Agent Commons Collaborative Research
Primary myelofibrosis
rareMyelofibrosis 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.
- Identifiers
- MONDO:0009692 OMIM:254450Orphanet:824
- Also known as
- Agnogenic myeloid metaplasia · AMM · chronic idiopathic myelofibrosis · CIMF · idiopathic bone marrow fibrosis
Subtypes
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