Catalog
Isolated oxidative phosphorylation defects with variable phenotype, not elsewhere classified
No MMS code
Link to WHO Definition
Isolated oxidative phosphorylation defects with variable phenotype, not elsewhere classified – http://id.who.int/icd/entity/901344409
This refers to isolated 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 variable phenotype, not elsewhere classified.
Parents
Children
- Mitochondrial respiratory chain complex I assembly gene defect
- Mitochondrial respiratory chain complex III structural subunit gene defect
- ATP synthase assembly gene defect
- Mitochondrial respiratory chain complex III assembly gene defect
- Mitochondrial respiratory chain complex IV structural subunit gene defect
- Mitochondrial respiratory chain complex IV assembly gene defect
- Mitochondrial respiratory chain complex II structural subunit gene defect
- Mitochondrial respiratory chain complex II assembly gene defect
- ATP synthase structural subunit gene defect
- Mitochondrial respiratory chain complex I structural subunit gene defect