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Progressive external ophthalmoplegia with mitochondrial DNA deletions

MONDO:0000090

Also known as: progressive external ophthalmoplegia with mtDNA deletions

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

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Sub-types

Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2 (1) Autosomal dominant progressive external ophthalmoplegia (0) Mitochondrial DNA deletion syndrome with progressive myopathy (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4 (0) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5 (0) Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6 (0)

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! 39 Not yet recruiting 12 Not yet finished but already full! 12 Completed 16 Terminated 2
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