Mitochondrial disease
MONDO:0044970132 clinical trials for this condition and its sub-types, 40 tagged with Mitochondrial disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Mitochondrial disease
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Inborn mitochondrial metabolism disorder 59 trials · 127 incl. sub-types
14 sub-types
- Mitochondrial oxidative phosphorylation disorder 3 trials · 58 incl. sub-types Sub-types →
- Inborn mitochondrial myopathy 18 trials · 45 incl. sub-types Sub-types →
- Pyruvate dehydrogenase deficiency 2 trials · 4 incl. sub-types Sub-types →
- Histiocytoid cardiomyopathy 3 trials Sub-types →
- Fumaric aciduria 2 trials
- OPA1-related optic atrophy with or without extraocular features 1 trial Sub-types →
- Inherited lipoic acid biosynthesis defect 0 trials · 1 incl. sub-types Sub-types →
- Multiple acyl-CoA dehydrogenase deficiency 1 trial Sub-types →
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome 0 trials
- HSD10 mitochondrial disease 0 trials Sub-types →
- Hypotonia-cystinuria syndrome 0 trials Sub-types →
- Mitochondrial membrane transport disorder 0 trials Sub-types →
- Mitochondrial pyruvate carrier deficiency 0 trials
- Oxoglutaricaciduria 0 trials
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1 sub-type
- Optic atrophy 9 0 trials
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Bjornstad syndrome 0 trials
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GRACILE syndrome 0 trials
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4 sub-types
- Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome 0 trials
- Optic atrophy 8 0 trials
- Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 0 trials
- Optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant 0 trials
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Ethylmalonic encephalopathy 0 trials
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Pure mitochondrial myopathy 0 trials
Most studied deeper sub-types
Leber hereditary optic neuropathy
(18)
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 DNA depletion syndrome, myopathic form
(4)
Mitochondrial neurogastrointestinal encephalomyopathy
(4)
Mitochondrial respiratory chain complex deficiency
(4)
Progressive external ophthalmoplegia
(4)
Autosomal dominant optic atrophy, classic form
(3)
Coenzyme Q10 deficiency
(3)
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
(3)
Mitochondrial DNA depletion syndrome
(3)
Mitochondrial DNA depletion syndrome 4a
(3)
Mitochondrial encephalomyopathy
(3)
Mitochondrial trifunctional protein deficiency
(3)
Myopathy, lactic acidosis, and sideroblastic anemia
(3)