All diseases

OMIM ID
608957
OMIM term:
CD8 DEFICIENCY, FAMILIAL
Alternative terms:

(∗) Location:
2p11.2  
(†) Associated OMIM genes:
CD8A  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/t5rww92r