Complex I deficiency [DS:
H00473]
Complex II deficiency [DS:
H02005]
Complex III deficiency [DS:
H02086]
COX deficiency [DS:
H01368]
Combined oxidative phosphorylation deficiency [DS:
H00891]
ATP synthase deficiency [DS:
H01369]
Mitochondrial DNA depletion syndrome [DS:
H00469]
MLASA [DS:
H00898]
MELAS syndrome [DS:
H01347]
Leigh syndrome [DS:
H01354]
Kearns-Sayre syndrome [DS:
H01355]
Leber hereditary optic atrophy [DS:
H00068]
LDYT [DS:
H01365]
Mitochondrial phosphate carrier deficiency [DS:
H01348]
Progressive external ophthalmoplegia [DS:
H01118]
MERRF syndrome [DS:
H01356]
GRACILE syndrome [DS:
H02007]
Infantile liver failure [DS:
H01367]
MIRAS [DS:
H01384]
Multiple mitochondrial dysfunctions syndrome [DS:
H01894]
Diseases of the TCA cycle [DS:
H01022]
Disorders of mitochondrial fatty acid oxidation [DS:
H00525]
Mohr-Tranebjaerg syndrome [DS:
H00989]
Bjornstad syndrome [DS:
H00820]
