muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
B3GALNT2 Causal
29791932 23453667
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11.
5 View disease cluster →
Kenny-caffey syndrome 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. Walker-warburg syndrome 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2. Nonsyndromic intellectual disability 1 shared geneB3GALNT2 Related via 1 shared gene including B3GALNT2.