Parent term(s)

mitochondrial myopathy +

Term with siblings

chronic progressive external ophthalmoplegia +

isolated mitochondrial myopathy
mitochondrial encephalomyopathy +
myopathy, lactic acidosis, and sideroblastic anemia +

Child term(s)

autosomal dominant progressive external ophthalmoplegia 1

autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2

autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3

autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4

autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5

autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6

autosomal recessive progressive external ophthalmoplegia 1

autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2

autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3

autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4

autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5

Kearns-Sayre syndrome

denotes an 'is-a' relationship