Myasthenic syndrome, congenital, 3c, associated with acetylcholine receptor deficiency

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Subtype of: Congenital myasthenic syndrome · Myasthenic syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency
MONDO_0018940
CHRND Unknown
16916845 18398509
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myasthenic syndrome, congenital, 3c, associated with acetylcholine receptor deficiency.
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Myasthenic syndrome, congenital, 3b, fast-channel 1 shared geneCHRND Related via 1 shared gene including CHRND. Multiple pterygium syndrome, lethal type 1 shared geneCHRND Related via 1 shared gene including CHRND. Paralysis 1 shared geneCHRND Related via 1 shared gene including CHRND. Postsynaptic congenital myasthenic syndrome 1 shared geneCHRND Related via 1 shared gene including CHRND. Blepharoptosis 1 shared geneCHRND Related via 1 shared gene including CHRND.