Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a13

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Subtype of: Congenital muscular dystrophy due to dystroglycanopathy · Muscular dystrophy · Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13
MONDO_0000171MONDO_0014120
B3GNT2 Unknown
23359570 23877401
Open Targets
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13
MONDO_0000171MONDO_0014120
B4GAT1 Causal
23217742 23359570 23877401
ClinGen, Open Targets
All2 Causal1 Unknown2
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. Graves disease 1 shared geneB3GNT2 Related via 1 shared gene including B3GNT2. Breast neoplasms 1 shared geneB4GAT1 Related via 1 shared gene including B4GAT1. Rheumatoid arthritis 1 shared geneB3GNT2 Related via 1 shared gene including B3GNT2.