Congenital myasthenic syndrome 2C

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Subtype of: Congenital myasthenic syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
congenital myasthenic syndrome 2C
MONDO:0014582
CHRNB1 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital myasthenic syndrome 2C.
5 View disease cluster →
Congenital myasthenic syndrome 2A 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1. Congenital myasthenic syndrome, monoallelic 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1. Congenital myasthenic syndrome, biallelic 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1. Myasthenic syndrome, congenital, 2c, associated with acetylcholine receptor deficiency 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1. Postsynaptic congenital myasthenic syndrome 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1.