All diseases

OMIM ID
177820
OMIM term:
PSEUDO-VON WILLEBRAND DISEASE; VWDP
Alternative terms:
BLEEDING DISORDER, PLATELET-TYPE, 3; BDPLT3
VON WILLEBRAND DISEASE, PLATELET-TYPE
(∗) Location:
17p13.2  
(†) Associated OMIM genes:
GP1BA  
(‡) Associated MGI genes:

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