Neutral Lipid Storage Disease With Myopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1853136
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Genes

6 genes associated with the disease Neutral Lipid Storage Disease With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABHD5 abhydrolase domain containing 5
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
PNPLA2 patatin-like phospholipase domain containing 2
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5