Hepatic Amyloidosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A form of amyloidosis that affects the liver. (Human Phenotype Ontology, HP_0012280)
External Link https://www.disgenet.org/browser/0/1/0/C0267839
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Genes

4 genes associated with the disease Hepatic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOA1 apolipoprotein A-I
LPA lipoprotein, Lp(a)
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A