autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5

Summary
Synonym
  • PEOB5
  • autosomal recessive progressive external ophthalmoplegia 5
Definition
A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the TOP3A gene on chromosome 17p11.2.
Super Class
autosomal recessive disease chronic progressive external ophthalmoplegia
Disease Ontology
DOID:0111524
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7156 TOP3A DNA topoisomerase III alpha

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024