- OMIM ID
-
601399
- OMIM term:
- PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
- Alternative terms:
-
FPDMM
PLATELET DISORDER, ASPIRIN-LIKE
THROMBOCYTOPENIA, FAMILIAL, WITH PROPENSITY TO ACUTE MYELOGENOUS LEUKEMIA; FPD/AML
- (∗) Location:
- 21q22.12
- (†) Associated OMIM genes:
- RUNX1
- (‡) Associated MGI genes:
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