All diseases

OMIM ID
220110
OMIM term:
MITOCHONDRIAL COMPLEX IV DEFICIENCY
Alternative terms:
CYTOCHROME c OXIDASE DEFICIENCY
COX DEFICIENCY
(∗) Location:
12q13.12   19q13.12   2q11.2   2q33.3  
(†) Associated OMIM genes:
C12ORF62   C2ORF64   COX6B1   FASTKD2  
(‡) Associated MGI genes:
Sco2  

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* quick link - http://q.sanger.ac.uk/vco9bffx