Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions
rare- Identifiers
- MONDO:0000090
- Also known as
- progressive external ophthalmoplegia with mtDNA deletions
Subtypes
Disease Rare Not rare Subtypes
- Autosomal dominant progressive external ophthalmoplegia MONDO:0008003 5
- Mitochondrial DNA deletion syndrome with progressive myopathy MONDO:0014062 DNA2
- Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1 MONDO:0009783 POLG
- Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2 MONDO:0014656 RNASEH1
- Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3 MONDO:0014898 TK2
- Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4 MONDO:0014899 DGUOK
- Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5 MONDO:0020845 TOP3A
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 MONDO:0957993 RRM1
Projects
Including projects on subtypes.
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