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DOID:0111521 - autosomal dominant progressive external ophthalmoplegia 1
Disease Ontology Definition:A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG gene on chromosome 15q26.1.
Synonyms: PEOA1,
Echinobase Genes :
MIM:157640 - progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1; peoa1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee