autosomal recessive progressive external ophthalmoplegia 1

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Summary

Literature (0)

DOID:0111522 - autosomal recessive progressive external ophthalmoplegia 1

Disease Ontology Definition:A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the POLG gene on chromosome 15q26.1.

Synonyms: PEOB1

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: polg

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), chronic progressive external ophthalmoplegia (is_a)