All diseases

OMIM ID
605735
OMIM term:
BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12
Alternative terms:
PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET
PGHS1 DEFICIENCY
PLATELET CYCLOOXYGENASE 1 DEFICIENCY
PLATELET COX1 DEFICIENCY
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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