Congenital muscular dystrophies

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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • congenital muscular dystrophies
MONDO_0013178
B3GALNT2 Unknown
23453667
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital muscular dystrophies.
5 View disease cluster →
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a11 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2. Kenny-caffey syndrome 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2. Muscular dystrophy-dystroglycanopathy 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2. Congenital muscular dystrophy due to dystroglycanopathy 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2. Muscle eye brain disease 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2.