# combined oxidative phosphorylation defect type 25

> human disease

**Wikidata**: [Q55784910](https://www.wikidata.org/wiki/Q55784910)  
**Source**: https://4ort.xyz/entity/combined-oxidative-phosphorylation-defect-type-25


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Novel, compound heterozygous, single-nucleotide variants in MARS2 associated with developmental delay, poor growth, and sensorineural hearing loss
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)