All diseases

OMIM ID
608106
OMIM term:
IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5
Alternative terms:

(∗) Location:
12q24.11  
(†) Associated OMIM genes:
UNG  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/e1ecbv3f