Myasthenic syndrome, congenital, 7a, presynaptic, and distal motor neuropathy, autosomal dominant

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Congenital myasthenic syndrome · Myasthenic syndrome · Presynaptic congenital myasthenic syndrome
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Myasthenic syndrome, congenital, 7A, presynaptic, and distal motor neuropathy, autosomal dominant
MONDO_0018940
SYT2 Unknown
25192047 26519543 30533528 33105646 33320396 34037996
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Myasthenic syndrome, congenital, 7a, presynaptic, and distal motor neuropathy, autosomal dominant.
5 View disease cluster →
Congenital myasthenic syndrome 7 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.