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Summary Literature (6)
MIM:160800 - MYOTONIA CONGENITA, AUTOSOMAL DOMINANT

Xenbase Genes: clcn1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008055 - myotonia congenita, autosomal dominant
MONDO:0009710 - Thomsen and Becker disease

Disease Ontology (DO):
DOID:0081336 - Thomsen disease
DOID:2106 - myotonia congenita