Progressive external ophthalmoplegia with mitochondrial DNA deletions
MONDO:0000090Also known as: progressive external ophthalmoplegia with mtDNA deletions
20 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal dominant progressive external ophthalmoplegia
(1)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
(1)
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
(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)