Mitochondrial disease
MONDO:0044970128 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Inborn mitochondrial metabolism disorder
(58)
Leber hereditary optic neuropathy
(18)
Inborn mitochondrial myopathy
(16)
MELAS syndrome
(13)
Leigh syndrome
(9)
Barth syndrome
(5)
Kearns-Sayre syndrome
(5)
Maternally-inherited diabetes and deafness
(5)
MERRF syndrome
(5)
Deafness, aminoglycoside-induced
(4)
Mitochondrial neurogastrointestinal encephalomyopathy
(4)
Mitochondrial respiratory chain complex deficiency
(4)
Autosomal dominant optic atrophy, classic form
(3)
Coenzyme Q10 deficiency
(3)
Histiocytoid cardiomyopathy
(3)
Mitochondrial DNA depletion syndrome
(3)
Mitochondrial DNA depletion syndrome 4a
(3)
Mitochondrial DNA depletion syndrome, myopathic form
(3)
Mitochondrial encephalomyopathy
(3)
Mitochondrial oxidative phosphorylation disorder
(3)