Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
MONDO:0024528Any autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.
Also known as: PEOA1, POLG autosomal dominant progressive external ophthalmoplegia, autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1, progressive external ophthalmoplegia, autosomal dominant 1
19 clinical trials for this condition and its sub-types.
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Disease
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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)