Search Ontology:
Human Disease

autosomal dominant progressive external ophthalmoplegia 1

Term ID
DOID:0111521
Synonyms
  • PEOA1
Definition
A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG gene on chromosome 15q26.1. https://www.ncbi.nlm.nih.gov/pubmed/11431686
References
Ontology
Human Disease   ( DOID:0111521 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models