Table B.

OMIM Entries for RUNX1 Familial Platelet Disorder with Associated Myeloid Malignancies (View All in OMIM)

151385RUNT-RELATED TRANSCRIPTION FACTOR 1; RUNX1
601399PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM

From: RUNX1 Familial Platelet Disorder with Associated Myeloid Malignancies

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