Concept information
Término preferido
Mitochondrial Diseases
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Conceptos específicos
- Carbamoyl-Phosphate Synthase I Deficiency Disease
- Cytochrome-c Oxidase Deficiency
- Friedreich Ataxia
- Leigh Disease
- Mitochondrial Myopathies
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency
- Optic Atrophy, Autosomal Dominant
- Optic Atrophy, Hereditary, Leber
- Pyruvate Carboxylase Deficiency Disease
- Pyruvate Dehydrogenase Complex Deficiency Disease
Etiquetas alternativas
- Mitochondrial Disorders
En otras lenguas
-
francés
-
Mitochondriopathies
URI
http://data.loterre.fr/ark:/67375/JVR-QV6F96CB-Q
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