Metabolic Disorder

Mitochondrial Diseases

AMW:DIS:180047

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.

Pathology clinical

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Mitochondrial Diseases has parent Metabolic Diseases

Mitochondrial Myopathies has parent Mitochondrial Diseases

Leigh Disease has parent Mitochondrial Diseases

Pyruvate Carboxylase Deficiency Disease has parent Mitochondrial Diseases

Pyruvate Dehydrogenase Complex Deficiency Disease has parent Mitochondrial Diseases

Carbamoyl-Phosphate Synthase I Deficiency Disease has parent Mitochondrial Diseases

Friedreich Ataxia has parent Mitochondrial Diseases

Optic Atrophy, Autosomal Dominant has parent Mitochondrial Diseases

Optic Atrophy, Hereditary, Leber has parent Mitochondrial Diseases

Multiple Acyl Coenzyme A Dehydrogenase Deficiency has parent Mitochondrial Diseases

Cytochrome-c Oxidase Deficiency has parent Mitochondrial Diseases

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