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PedAM

Pediatric Disease Annotations & Medicines




Disease primary myelofibrosis
Phenotype C0001815|idiopathic myelofibrosis
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PubMedID- 19785025 Chronic idiopathic myelofibrosis (cim) with myeloid metaplasia is a myeloproliferative disorder characterized by leukoerythroblastosis, tear drop erythrocytes, extra-medullary hematopoesis (emh), and varying degree of myelofibrosis.
PubMedID- 23208557 This mutation has been identified in most polycythemia vera (pv) patients, approximately half of essential thrombocythemia (et) and chronic idiopathic myelofibrosis with extramedullary hematopoiesis (cimf) patients, and in a substantial population of other chronic myeloproliferative disease (cmpd) patients [40].

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