All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01740 - cytochrome-c oxidase deficiency (mitochondrial complex IV deficiency) 220110 - - - APOPT1, COA5, COX10, COX14, COX20, COX6B1, FASTKD2, PET100, SCO1, TACO1 - -
04419 CEMCOX-3 cardioencephalomyopathy?, fatal infantile, due to cytochrome C oxidase deficiency, type 3 (CEMCOX-3) 616500 - - - COA5 - -
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