autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 (DOID:0111525)
Alliance: disease page
Synonyms: autosomal dominant progressive external ophthalmoplegia 4; PEOA4
Alt IDs: OMIM:610131
Definition: A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the POLG2 gene on chromosome 17q23.3.