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Platelet Disorder, Familial, with Associated Myeloid Malignancy MeSH Supplementary Concept Data 2025


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 Numbers
0
Heading Mapped to
*Blood Platelet Disorders
*Leukemia, Myeloid, Acute
*Blood Coagulation Disorders, Inherited
Frequency
12
Date of Entry
2012/11/05
Revision Date
2012/11/05
Platelet Disorder, Familial, with Associated Myeloid Malignancy Preferred
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