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Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5

MONDO:0013117

Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RRM2B gene.

Also known as: RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions, progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5, PEOA5, progressive external ophthalmoplegia, autosomal dominant 5

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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