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autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3 (DOID:0111523)
Alliance: disease page
Synonyms: autosomal recessive progressive external ophthalmoplegia 3; PEOB3
Alt IDs: OMIM:617069
Definition: A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in TK2 on chromosome 16q21.


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
01/31/2023
MGI 6.22
The Jackson Laboratory