Myasthenic syndrome, congenital, 2c, associated with acetylcholine receptor deficiency

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Subtype of: Congenital myasthenic syndrome · Congenital myasthenic syndrome 2C · Myasthenic syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency
MONDO_0018940
CHRNB1 Unknown
10562302
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myasthenic syndrome, congenital, 2c, associated with acetylcholine receptor deficiency.
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Congenital myasthenic syndrome 2C 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1. 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. Postsynaptic congenital myasthenic syndrome 1 shared geneCHRNB1 Related via 1 shared gene including CHRNB1.