Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Mitochondrial Diseases
Description
Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. MeSH
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Subtype Terms (10)
Carbamoyl-Phosphate Synthase I Deficiency Disease
1 approved drug
Cytochrome-c Oxidase Deficiency
Friedreich Ataxia
35 drugs (18 approved, 17 experimental)
Leigh Disease
3 drugs (1 approved, 2 experimental)
Mitochondrial Myopathies
10 drugs (4 approved, 6 experimental)
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
1 experimental drug
Optic Atrophy, Autosomal Dominant
Optic Atrophy, Hereditary, Leber
18 drugs (2 approved, 16 experimental)
Pyruvate Carboxylase Deficiency Disease
2 drugs (1 approved, 1 experimental)
Pyruvate Dehydrogenase Complex Deficiency Disease
2 drugs (1 approved, 1 experimental)
Approved Indicated Drugs (1)
Phase 4 Indicated Drugs (6)
Phase 3 Indicated Drugs (3)
Other Experimental Indicated Drugs (11)
Organization Involved with Phase 4 Indications (2)
Organization Involved with Phase 3 Indications (6)
Organization Involved with Phase 2 Indications (14)
Organization Involved with Phase 1 Indications (8)
Organization Involved with Other Experimental Indications (10)
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UMLS Data
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