Mitochondrial oxidative phosphorylation disorders with no known genetic basis (Q87783): Difference between revisions
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| description / pt-br | description / pt-br | ||
Trata-se de distúrbios da via metabólica em que as mitocôndrias nas células usam sua estrutura, enzimas e energia liberada pela oxidação de nutrientes para corrigir o ATP. Este diagnóstico não tem base genética conhecida. | |||
| description / en | description / en | ||
This refers to disorders of the metabolic pathway in which the mitochondria in cells use their structure, enzymes, and energy released by the oxidation of nutrients to reform ATP. This diagnosis is with no known genetic basis. | |||
Revision as of 13:42, 15 August 2026
This refers to disorders of the metabolic pathway in which the mitochondria in cells use their structure, enzymes, and energy released by the oxidation of nutrients to reform ATP. This diagnosis is with no known genetic basis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_670455494 |
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| English | Mitochondrial oxidative phosphorylation disorders with no known genetic basis |
This refers to disorders of the metabolic pathway in which the mitochondria in cells use their structure, enzymes, and energy released by the oxidation of nutrients to reform ATP. This diagnosis is with no known genetic basis. |
