All diseases

OMIM ID
233650
OMIM term:
COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS; CCHIDG
Alternative terms:

(∗) Location:
11p12  
(†) Associated OMIM genes:
RAG1   RAG2  
(‡) Associated MGI genes:

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