Term Name:	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
Synonyms:	autosomal dominant progressive external ophthalmoplegia 2, PEOA2
Definition:	A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the SLC25A4 gene on chromosome 4q35.1.
Ontology:	Human Disease [DOID:0111517]   ( DOID:0111517 )