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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 dominant disease
Charcot-Marie-tooth disease, axonal, type 2DD
rare
Identifiers
MONDO:0054833
OMIM:618036
Orphanet:521414
Causal genes
ATP1A1
Part of
Charcot-Marie-Tooth disease type 2
Autosomal dominant disease
Also known as
CMT2DD
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