Walker-warburg syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WALKER-WARBURG CONGENITAL MUSCULAR DYSTROPHY
C0265221
FKRP Causal — Disgenet
FKTN Causal — Disgenet
POMT1 Causal — Disgenet
RXYLT1 Causal — Disgenet
All16 Causal4 Unknown16
Related Diseases Diseases that share the most curated genes with Walker-warburg syndrome.
5 View disease cluster →
Muscle eye brain disease 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 6 shared genesGMPPB, LARGE1, CRPPA, POMGNT1, FKRP, B3GALNT2 Related via 6 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 9 shared genesDAG1, GMPPB, CRPPA, POMT1, POMT2, POMGNT1, FKRP, FKTN, POMK Related via 9 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.