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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Autosomal genetic disease
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Autosomal recessive disease
Autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
rare
Identifiers
MONDO:0033850
Orphanet:521411
Causal genes
SCO2
Part of
Autosomal recessive disease
Disorder of copper metabolism
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