Myopathy caused by variation in POMGNT1

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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • myopathy caused by variation in POMGNT1
POMGNT1 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Myopathy caused by variation in POMGNT1.
5 View disease cluster →
Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b3 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Congenital muscular dystrophy due to dystroglycanopathy 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Muscle eye brain disease 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1. Walker-warburg syndrome 1 shared genePOMGNT1 Related via 1 shared gene including POMGNT1.