autosomal recessive progressive external ophthalmoplegia 1 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive progressive external ophthalmoplegia 1 (DOID:0111522)
Alliance: disease page
Synonyms: PEOB1
Alt IDs: OMIM:258450
Definition: A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the POLG gene 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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