MeSH Browser

MeSH Supplementary: Platelet Disorder, Familial, with Associated Myeloid Malignancy
Unique ID: C563324
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563324
Entry Term(s): FPDAML; FPDMM; Platelet Disorder, Aspirin-Like; Thrombocytopenia, Familial, with Propensity to Acute Myelogenous Leukemia
Registry Number: 0
Heading Mapped to: *Blood Platelet Disorders; *Leukemia, Myeloid, Acute; *Blood Coagulation Disorders, Inherited
Frequency: 12
Date of Entry: 2012/11/05

Platelet Disorder, Familial, with Associated Myeloid Malignancy MeSH Supplementary Concept Data 2024