Mitochondrial Diseases D028361

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
31 drugs (16 approved, 15 experimental)

Leigh Disease
3 drugs (1 approved, 2 experimental)


Phase 3 Indicated Drugs (2)


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UMLS Data


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