All diseases

OMIM ID
227600
OMIM term:
FACTOR X DEFICIENCY
Alternative terms:
F10 DEFICIENCY
STUART-PROWER FACTOR DEFICIENCY
(∗) Location:
13q34  
(†) Associated OMIM genes:
F10  
(‡) Associated MGI genes:
F10  

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