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Summary Literature (5)
MIM:255700 - MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE

Xenbase Genes: clcn1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009710 - Thomsen and Becker disease
MONDO:0009715 - stomodeal lumen

Disease Ontology (DO):
DOID:2106 - myotonia congenita