About   Help   FAQ
Disease Ontology Browser
autosomal recessive progressive external ophthalmoplegia 1 (DOID:0111522)
Alliance: disease page
Synonyms: autosomal recessive progressive external ophthalmoplegia 1; PEOB1
Alt IDs: OMIM:258450
Definition: A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound 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 Notice
Send questions and comments to User Support.
last database update
02/11/2020
MGI 6.14
The Jackson Laboratory