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Disease association ontology term - MONDO:0024528 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1

Term summary

ID
MONDO:0024528
Name
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
Ontology or CV name
Disease association
Definition
Any autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.

Parents

Annotation

Disease association

MONDO:0024528 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1

References:

Genes: