All diseases

OMIM ID
613225
OMIM term:
FACTOR XIII, A SUBUNIT, DEFICIENCY OF
Alternative terms:

(∗) Location:
6p25.1  
(†) Associated OMIM genes:
F13A1  
(‡) Associated MGI genes:
F13a1  

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* quick link - http://q.sanger.ac.uk/olnu1evo