# mitochondrial complex III deficiency nuclear type 3

> mitochondrial complex III deficiency that has material basis in homozygous mutation in the UQCRB gene on chromosome 8q22

**Wikidata**: [Q26492807](https://www.wikidata.org/wiki/Q26492807)  
**Source**: https://4ort.xyz/entity/mitochondrial-complex-iii-deficiency-nuclear-type-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)