# combined oxidative phosphorylation defect type 30

> human disease

**Wikidata**: [Q55785062](https://www.wikidata.org/wiki/Q55785062)  
**Source**: https://4ort.xyz/entity/combined-oxidative-phosphorylation-defect-type-30


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)