Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Progressive external ophthalmoplegia with mitochondrial DNA deletions · Autosomal recessive progressive external ophthalmoplegia
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
Any autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the TK2 gene.
This condition has no sub-types.