All diseases

OMIM ID
604377
OMIM term:
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY
Alternative terms:

(∗) Location:
22q13.33  
(†) Associated OMIM genes:
SCO2  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/3cr3outg