All diseases

OMIM ID
612783
OMIM term:
IMMUNE DYSFUNCTION WITH T-CELL INACTIVATION DUE TO CALCIUM ENTRY DEFECT 2
Alternative terms:

(∗) Location:
11p15.4  
(†) Associated OMIM genes:
STIM1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/cdt7ed5w