Myotonia congenita

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
THOMSEN AND BECKER DISEASE
614MONDO:0009710
CLCN1 Unknown
20301529
GWAS catalog, Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myotonia congenita.
5 View disease cluster →
Congenital myotonia 1 shared geneCLCN1 Related via 1 shared gene including CLCN1. Becker generalized myotonia 1 shared geneCLCN1 Related via 1 shared gene including CLCN1. Hyperkalemic periodic paralysis 1 shared geneCLCN1 Related via 1 shared gene including CLCN1. Smith-lemli-opitz syndrome 1 shared geneCLCN1 Related via 1 shared gene including CLCN1. Metachromatic leukodystrophy 1 shared geneCLCN1 Related via 1 shared gene including CLCN1.