About   Help   FAQ
Disease Ontology Browser
autosomal dominant progressive external ophthalmoplegia 1 (DOID:0111521)
Alliance: disease page
Synonyms: PEOA1
Alt IDs: OMIM:157640
Definition: A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in POLG on chromosome 15q26.1.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
03/14/2023
MGI 6.22
The Jackson Laboratory