# mitochondrial complex III deficiency nuclear type 7

> mitochondrial complex III deficiency that has material basis in homozygous mutation in the UQCC2 gene on chromosome 6p21

**Wikidata**: [Q26492811](https://www.wikidata.org/wiki/Q26492811)  
**Source**: https://4ort.xyz/entity/mitochondrial-complex-iii-deficiency-nuclear-type-7


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)