neutral lipid storage myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neutral lipid storage myopathy
PNPLA2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neutral lipid storage myopathy.
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Fuchs endothelial dystrophy 1 shared genePNPLA2 Related via 1 shared gene including PNPLA2. Ventricular dysfunction 1 shared genePNPLA2 Related via 1 shared gene including PNPLA2. Hypertrophy 1 shared genePNPLA2 Related via 1 shared gene including PNPLA2. Left ventricular disease 1 shared genePNPLA2 Related via 1 shared gene including PNPLA2. Keratoconus 1 shared genePNPLA2 Related via 1 shared gene including PNPLA2.