Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2

MONDO:0014656

Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RNASEH1 gene.

Also known as: RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions, progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2, PEOB2, progressive external ophthalmoplegia, autosomal recessive 2

19 clinical trials for this condition and its sub-types, 0 tagged with Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2 itself.

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↑ Progressive external ophthalmoplegia with mitochondrial DNA deletions (2) ↑ Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (0)

Including sub-types (19) Tagged with Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2 (0)

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