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Platelet Disorder, Familial, with Associated Myeloid Malignancy [Supplementary Concept]

Date introduced: November 5, 2012

MeSH Unique ID: C563324

Heading Mapped to:

Entry Terms:

  • FPDAML
  • FPDMM
  • Platelet Disorder, Aspirin-Like
  • Thrombocytopenia, Familial, with Propensity to Acute Myelogenous Leukemia

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