muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13

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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 A13
B4GAT1 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13.
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Muscle eye brain disease 1 shared geneB4GAT1 Related via 1 shared gene including B4GAT1. Walker-warburg syndrome 1 shared geneB4GAT1 Related via 1 shared gene including B4GAT1. Breast neoplasms 1 shared geneB4GAT1 Related via 1 shared gene including B4GAT1.