Congenital myasthenic syndrome 7

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Subtype of: Congenital myasthenic syndrome
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • congenital myasthenic syndrome 7
MONDO:0014468
SYT2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Congenital myasthenic syndrome 7.
5 View disease cluster →
Myasthenic syndrome, congenital, 7a, presynaptic, and distal motor neuropathy, autosomal dominant 1 shared geneSYT2 Related via 1 shared gene including SYT2. Presynaptic congenital myasthenic syndrome 1 shared geneSYT2 Related via 1 shared gene including SYT2. Thyroid gland neoplasms 1 shared geneSYT2 Related via 1 shared gene including SYT2. Congenital myasthenic syndrome 1 shared geneSYT2 Related via 1 shared gene including SYT2. Myasthenic syndrome 1 shared geneSYT2 Related via 1 shared gene including SYT2.