All diseases

OMIM ID
153670
OMIM term:
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2
Alternative terms:

(∗) Location:
17p13.2  
(†) Associated OMIM genes:
GP1BA  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/qxwluuj9