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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)
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last database update
MGI 6.22
The Jackson Laboratory