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Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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POLR3B-related disorder
Charcot-Marie-Tooth disease, demyelinating, IIA 1I
rare
Identifiers
MONDO:0030677
OMIM:619742
Part of
Charcot-Marie-Tooth disease
POLR3B-related disorder
Also known as
Charcot-Marie-Tooth disease neuropathy, IIA 1I · CMT1I
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