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- neuropathy, ataxia, and retinitis pigmentosa condition summary
Related classification: Mitochondrial Diseases
Related genes and chromosomes:
- mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes condition summary
Related classification: Mitochondrial Diseases
Related genes and chromosomes:
- Leber hereditary optic neuropathy condition summary
Related classification: Mitochondrial Diseases
Related genes and chromosomes:
- myoclonic epilepsy with ragged-red fibers condition summary
Related classification: Mitochondrial Diseases
Related genes and chromosomes:
- MT-TH gene summary
Official name: mitochondrially encoded tRNA histidine
Found: ...without other common signs of mitochondrial disease such as neurological abnormalities....
- Kearns-Sayre syndrome condition summary
Related classification: Mitochondrial Diseases
- cytochrome c oxidase deficiency condition summary
Related classification: Mitochondrial Diseases
- progressive external ophthalmoplegia condition summary
Related classification: Mitochondrial Diseases
Related genes and chromosomes:
- Leigh syndrome condition summary
Related classification: Mitochondrial Diseases
Related genes and chromosomes:
- MT-ND5 gene summary
Official name: mitochondrially encoded NADH dehydrogenase 5
Found: ...MELAS in combination with other mitochondrial diseases. For example, researchers have...
- mitochondrial DNA summary
Found related term: ...The severity of many mitochondrial disorders is thought to be associated with...
- MT-ATP6 gene summary
Official name: mitochondrially encoded ATP synthase 6
Found related term: ...DNA. The severity of some mitochondrial disorders is associated with the percentage...
- MT-TK gene summary
Official name: mitochondrially encoded tRNA lysine
Found related term: ...and some features of another mitochondrial disorder called mitochondrial encephalomyopathy,...
- Can changes in mitochondrial DNA affect health and development? in the Handbook
Found: ...offers a basic introduction to mitochondrial disease.
- ataxia neuropathy spectrum condition summary
Related classification: Mitochondrial Diseases
- carbamoyl phosphate synthetase I deficiency condition summary
Related classification: Mitochondrial Diseases
- childhood myocerebrohepatopathy spectrum condition summary
Related classification: Mitochondrial Diseases
- deoxyguanosine kinase deficiency condition summary
Related classification: Mitochondrial Diseases
- Friedreich ataxia condition summary
Related classification: Mitochondrial Diseases
- mitochondrial neurogastrointestinal encephalopathy disease condition summary
Related classification: Mitochondrial Diseases