Any autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the TK2 gene.
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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 2
MONDO:0014656
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4
MONDO:0014899
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
MONDO:0020845