All diseases

OMIM ID
613235
OMIM term:
FACTOR XIII, B SUBUNIT, DEFICIENCY OF
Alternative terms:

(∗) Location:
1q31.3  
(†) Associated OMIM genes:
F13B  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/81nt9fkm