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



In Mondo Disease Ontology:
MONDO:0100083 - hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1

Human Disease Resources: OMIM

Xenbase Genes: runx1