/myotonia congenita, autosomal dominant

myotonia congenita, autosomal dominant

Rare Disease

MONDO:0008055

Also Known As

Thomsen and Becker diseaseThomsen diseaseThomsen's diseasecongenital myotonia, autosomal dominant formmyotonia congenita, autosomal dominantmyotonia congenita, dominantmyotonia Levior

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Associated Genes

CLCN1 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:160800 ↗

GARD

GARD:6176 ↗

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