Mitochondrial disease
MONDO:0044970124 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Inborn mitochondrial metabolism disorder
(57)
Leber hereditary optic neuropathy
(17)
Inborn mitochondrial myopathy
(15)
MELAS syndrome
(12)
Leigh syndrome
(7)
Barth syndrome
(4)
Deafness, aminoglycoside-induced
(4)
Kearns-Sayre syndrome
(4)
MERRF syndrome
(4)
Mitochondrial respiratory chain complex deficiency
(4)
Autosomal dominant optic atrophy, classic form
(3)
Histiocytoid cardiomyopathy
(3)
Maternally-inherited diabetes and deafness
(3)
Mitochondrial DNA depletion syndrome
(3)
Mitochondrial DNA depletion syndrome 4a
(3)
Mitochondrial DNA depletion syndrome, myopathic form
(3)
Mitochondrial encephalomyopathy
(3)
Mitochondrial neurogastrointestinal encephalomyopathy
(3)
Mitochondrial oxidative phosphorylation disorder
(3)
Mitochondrial trifunctional protein deficiency
(3)