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Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3

MONDO:0014898

Any autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the TK2 gene.

Also known as: PEOB3, TK2 autosomal recessive progressive external ophthalmoplegia, autosomal recessive progressive external ophthalmoplegia caused by mutation in TK2, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3; PEOB3, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 3, progressive external ophthalmoplegia, autosomal recessive 3

80 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Central nervous system disorder (97) Inborn mitochondrial metabolism disorder (57) Muscle tissue disorder (53) Inborn errors of metabolism (42) Mitochondrial disease (39)
Trials to join now! 38 Not yet recruiting 12 Not yet finished but already full! 12 Completed 16 Terminated 2
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