Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
rareAny autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the TK2 gene.
- Identifiers
- MONDO:0014898 OMIM:617069
- Causal genes
- TK2
- Part of
- Autosomal recessive progressive external ophthalmoplegiaProgressive external ophthalmoplegia with mitochondrial DNA deletions
- Also known as
- autosomal recessive progressive external ophthalmoplegia caused by mutation in TK2 · PEOB3 · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3; PEOB3 · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 3 · TK2 autosomal recessive progressive external ophthalmoplegia
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