Catalog
Mitochondrial oxidative phosphorylation disorders with no known genetic basis
No MMS code
Link to WHO Definition
Mitochondrial oxidative phosphorylation disorders with no known genetic basis – http://id.who.int/icd/entity/670455494
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.
Parents
Children
- Isolated mitochondrial respiratory chain complex IV deficiency
- Succinic acidaemia
- Autosomal recessive optic atrophy type 7
- Deafness - opticoacoustic nerve atrophy - dementia
- FASTKD2-related infantile mitochondrial encephalomyopathy
- Isolated mitochondrial respiratory chain complex II deficiency
- Isolated mitochondrial respiratory chain complex III deficiency
- Isolated mitochondrial respiratory chain complex I deficiency
- Zellweger-like syndrome without peroxisomal anomalies
- 5C53.25 Isolated ATP synthase deficiency