Autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
MONDO:00338500 clinical trials for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Autosomal recessive disease
(4)
Disease of genetic or genomic mechanism
(2)
Autosomal genetic disease
(0)
Disease by developmental or physiological process
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Disease by etiologic mechanism
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