|
ID
|
Abbreviation
|
Name
|
OMIM ID
|
Individuals
|
Phenotypes
|
Associated with genes
|
Associated tissues
|
Disease features
|
00012 |
220110 |
Mitochondrial complex IV deficiency, 220110 (3) |
220110 |
1 |
0 |
APOPT1, COA5, COA7, COX10, COX14, COX20, COX6B1, COX8A, FASTKD2, MT-CO1, MT-CO2, MT-CO3, MT-TL1, MT-TN, PET100, SCO1, SURF1, TACO1 |
- |
- |
00642 |
616500 |
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 |
616500 |
0 |
0 |
COA5 |
- |
- |
|