All diseases

OMIM ID
261000
OMIM term:
INTRINSIC FACTOR DEFICIENCY; IFD
Alternative terms:

(∗) Location:
11q12.1  
(†) Associated OMIM genes:
GIF  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/crf3s9y4