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PedAM

Pediatric Disease Annotations & Medicines




Disease splenomegaly
Phenotype C0029464|osteosclerosis
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PubMedID- 26185644 Primary myelofibrosis (pm) is a myeloproliferative disorder characterized by unexplained fibrosis in the bone marrow and osteosclerosis, extramedullary hematopoiesis with marked splenomegaly, and a leukoerythroblastic anemia.

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