Autosomal dominant progressive external ophthalmoplegia
MONDO:0008003Autosomal 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.
Follow this condition — get notified about new trialsSub-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)