Disease #00133

Official abbreviation FPDMM
Name Platelet disorder, familial, with associated myeloid malignancy
OMIM ID 601399
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RUNX1
Associated tissues -
Disease features -
Remarks -