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Summary Literature (0)
MIM:601399 - PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM

Xenbase Genes: runx1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0100083 - hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1