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 MC4DN mitochondrial complex IV deficiency (MCDN4) - - 17 17 APOPT1, COA5, COX10, COX14, COX20, COX5A, COX6A2, COX6B1, FASTKD2, PET100, SCO1, SURF1, TACO1 - -
05956 MC4DN20 mitochondrial complex IV deficiency, nuclear, type 20 (MC4DN20) 619064 AR - - COX5A - -
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