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Autosomal dominant progressive external ophthalmoplegia

MONDO:0008003

Autosomal dominant form of progressive external ophthalmoplegia.

Also known as: adPEO, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 1, progressive external ophthalmoplegia, autosomal dominant, PEOA1, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1

20 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) 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)

Broader categories

Disease (680) Metabolic disease (233) Nervous system disorder (231) Musculoskeletal system disorder (207) Hereditary disease (176) Central nervous system disorder (107) Inborn mitochondrial metabolism disorder (58) Muscle tissue disorder (56) Inborn errors of metabolism (45) Mitochondrial disease (40)

Trials to join now! 11 Not yet recruiting 2 Not yet finished but already full! 4 Completed 2 Terminated 1