All diseases

OMIM ID
610505
OMIM term:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3; COXPD3
Alternative terms:
ENCEPHALOMYOPATHY, RESPIRATORY FAILURE, AND LACTIC ACIDOSIS
CONCENTRIC CARDIOMYOPATHY, HYPOTONIA, AND LACTIC ACIDOSIS
(∗) Location:
12q14.1  
(†) Associated OMIM genes:
TSFM  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/m5lu4o6r