All diseases

OMIM ID
231200
OMIM term:
BERNARD-SOULIER SYNDROME; BSS
Alternative terms:
BLEEDING DISORDER, PLATELET-TYPE, 1; BDPLT1
PLATELET GLYCOPROTEIN Ib DEFICIENCY
GLYCOPROTEIN Ib, PLATELET, DEFICIENCY OF
VON WILLEBRAND FACTOR RECEPTOR DEFICIENCY BERNARD-SOULIER SYNDROME, TYPE A1, INCLUDED
BERNARD-SOULIER SYNDROME, TYPE B, INCLUDED
BERNARD-SOULIER SYNDROME, TYPE C, INCLUDED
(∗) Location:
17p13.2   22q11.21   3q21.3  
(†) Associated OMIM genes:
GP1BA   GP1BB   GP9  
(‡) Associated MGI genes:
Gp1ba   Gp1bb  

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