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Up to: Progressive external ophthalmoplegia with mitochondrial DNA deletions · Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RNASEH1 gene.
This condition has no sub-types.