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Myotonia congenita, autosomal dominant

MONDO:0008055

Also known as: Thomsen and Becker disease, Thomsen disease, myotonia congenita, autosomal dominant, myotonia congenita, dominant, myotonia Levior

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neuromuscular disease (98) Human disease (14) Thomsen and Becker disease (9) Hereditary neurological disease (5) Hereditary neuromuscular disease (3) Disease by molecular mechanism (2) Disease of genetic or genomic mechanism (2)
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