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Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Hereditary neuromuscular disease
Myotonia congenita, autosomal dominant
rare
Identifiers
MONDO:0008055
OMIM:160800
Causal genes
CLCN1
Part of
Thomsen and Becker disease
Hereditary neuromuscular disease
Also known as
myotonia congenita, dominant · Thomsen disease
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