# mitochondrial complex III deficiency nuclear type 9

> mitochondrial complex III deficiency that has material basis in homozygous mutation in the UQCC3 gene on chromosome 11q12

**Wikidata**: [Q26492813](https://www.wikidata.org/wiki/Q26492813)  
**Source**: https://4ort.xyz/entity/mitochondrial-complex-iii-deficiency-nuclear-type-9


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)