Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a9

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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, 9
  • Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A9
MONDO_0014683
DAG1 Unknown
12140559 21388311 22810924 24052401 25529582 25934851 26380289 35082294
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a9.
5 View disease cluster →
Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan 1 shared geneDAG1 Related via 1 shared gene including DAG1. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a 1 shared geneDAG1 Related via 1 shared gene including DAG1. Muscle eye brain disease 1 shared geneDAG1 Related via 1 shared gene including DAG1. Walker-warburg syndrome 1 shared geneDAG1 Related via 1 shared gene including DAG1. Limb-girdle muscular dystrophy 1 shared geneDAG1 Related via 1 shared gene including DAG1.