Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RNASEH1 gene.
Comprehensive, easy-to-understand information about this condition
Checking for content...
autosomal dominant progressive external ophthalmoplegia
MONDO:0008003
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
MONDO:0009783
mitochondrial DNA deletion syndrome with progressive myopathy
MONDO:0014062
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
MONDO:0014898
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4
MONDO:0014899
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
MONDO:0020845