All diseases

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

ID     

AscendingAbbreviation     

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 - -
00015 LS Leigh syndrome due to mitochondrial complex 1 deficiency, 256000 (3) 256000 0 0 BCS1L, COX10, COX15, FOXRED1, MT-ATP6, MT-TK, MT-TV, MT-TW, NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFAF2, NDUFAF6, NDUFS3, NDUFS4, NDUFS7, NDUFS8, SDHA, SURF1 - -