All diseases

3 entries on 1 page. Showing entries 1 - 3.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00016 252011 Mitochondrial complex II deficiency, 252011 (3) 252011 0 0 SDHA, SDHAF1, SDHD - -
00086 CMD1GG Cardiomyopathy, dilated, 1GG, 613642 (3) 613642 0 0 SDHA - -
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 - -