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DOID:0111520 - autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
Disease Ontology Definition:A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the TWNK gene on chromosome 10q24.31.
Synonyms: PEOA3, autosomal dominant progressive external ophthalmoplegia 3,
Xenbase Genes : twnk
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee