Mitochondrial DNA deletion syndrome with progressive myopathy
MONDO:0014062Also known as: mitochondrial DNA deletion syndrome with limb-girdle weakness, mtDNA deletion syndrome with limb-girdle weakness, mtDNA deletion syndrome with progressive myopathy, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 6, PEOA6, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6, progressive external ophthalmoplegia, autosomal dominant 6
19 clinical trials for this condition and its sub-types.
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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)