Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
MONDO:0020845Also known as: PEOB5, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5, progressive external ophthalmoplegia, autosomal recessive 5
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)