Muscle eye brain disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MUSCLE EYE BRAIN DISEASE
C0457133
POMGNT1 Causal — Disgenet
All15 Causal1 Unknown15
Related Diseases Diseases that share the most curated genes with Muscle eye brain disease.
5 View disease cluster →
Walker-warburg syndrome 14 shared genesDAG1, GMPPB, LARGE1, CRPPA, POMGNT2, POMT1, POMT2, POMGNT1, FKRP, FKTN, B3GALNT2, B4GAT1 +2 more Related via 14 shared genes including DAG1, GMPPB, LARGE1. Congenital muscular dystrophy due to dystroglycanopathy 7 shared genesGMPPB, LARGE1, CRPPA, POMGNT1, TSPAN1, FKRP, B3GALNT2 Related via 7 shared genes including GMPPB, LARGE1, CRPPA. Congenital muscular dystrophy 9 shared genesGMPPB, LARGE1, CRPPA, POMT1, POMT2, POMGNT1, FKRP, FKTN, POMK Related via 9 shared genes including GMPPB, LARGE1, CRPPA. Limb girdle muscular dystrophy 10 shared genesDAG1, GMPPB, CRPPA, POMT1, POMT2, POMGNT1, TSPAN1, FKRP, FKTN, POMK Related via 10 shared genes including DAG1, GMPPB, CRPPA. Muscular dystrophy 9 shared genesDAG1, GMPPB, LARGE1, CRPPA, POMT1, POMT2, POMGNT1, FKRP, FKTN Related via 9 shared genes including DAG1, GMPPB, LARGE1.