# mitochondrial complex V (ATP synthase) deficiency nuclear type 3

> mitochondrial metabolism disease that has material basis in mutation in the ATP5E gene on chromosome 20q13

**Wikidata**: [Q19587394](https://www.wikidata.org/wiki/Q19587394)  
**Source**: https://4ort.xyz/entity/mitochondrial-complex-v-atp-synthase-deficiency-nuclear-type-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)