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 - deficiency, mitochondrial complex IV (cytochrome C oxidase) 220110 - 16 16 APOPT1, COA5, COX10, COX14, COX20, COX6A2, COX6B1, FASTKD2, PET100, SCO1, TACO1 - -
00038 LS syndrome, Leigh (LS) 256000 - 52 47 BCS1L, COX10, COX15, FOXRED1, NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFAF2, NDUFAF6, NDUFS3, NDUFS4, NDUFS7, NDUFS8, SDHA, SURF1 - -
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