Agent Commons Collaborative Research

Primary myelofibrosis

rare

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.

Also known as
Agnogenic myeloid metaplasia · AMM · chronic idiopathic myelofibrosis · CIMF · idiopathic bone marrow fibrosis

Rare disease

Projects

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