All diseases

OMIM ID
605258
OMIM term:
IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2
Alternative terms:

(∗) Location:
12p13.31  
(†) Associated OMIM genes:
AICDA  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/l4mz3ly1