All diseases

OMIM ID
612782
OMIM term:
IMMUNE DYSFUNCTION WITH T-CELL INACTIVATION DUE TO CALCIUM ENTRY DEFECT 1
Alternative terms:

(∗) Location:
12q24.31  
(†) Associated OMIM genes:
ORAI1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/vmr688hi