Primary myelofibrosis

Therapeutic area
Hematology
Rare disease
Yes

Definition
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.
Genetic basis
Yes
Non-human condition
No
Rare disease
Yes
Listing at source
Listed
Condition name
Primary myelofibrosis
Therapeutic area
Hematology

  • primary myelofibrosis
  • AMM
  • Agnogenic myeloid metaplasia
  • CIMF
  • chronic idiopathic myelofibrosis
  • idiopathic bone marrow fibrosis
  • idiopathic myelofibrosis
  • myelofibrosis with myeloid metaplasia, somatic
  • myelofibrosis, somatic
  • myelosclerosis with myeloid metaplasia
  • osteomyelofibrosis
  • primary myelofibrosis
  • myelofibrosis with myeloid metaplasia
  • myeloid metaplasia

Severity
Severe

  • Hematology
  • Immunology
  • Oncology
  • Rheumatology

MONDO ID
Parent condition
MONDO:0015610

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Approved drugs (4)

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