# progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1

> human disease

**Wikidata**: [Q55782168](https://www.wikidata.org/wiki/Q55782168)  
**Source**: https://4ort.xyz/entity/progressive-external-ophthalmoplegia-with-mitochondrial-dna-deletions-autosomal-recessive-1


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)