All diseases

OMIM ID
212350
OMIM term:
SENGERS SYNDROME
Alternative terms:
MITOCHONDRIAL DNA DEPLETION SYNDROME 10 (CARDIOMYOPATHIC TYPE); MTDPS10
CARDIOMYOPATHY AND CATARACT
(∗) Location:
7q34  
(†) Associated OMIM genes:
AGK  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/y1l62e83