chronic hepatitis c Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice. (Human Disease Ontology, DOID_1883)
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Genes

6 genes associated with the disease chronic hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CCL3L1 chemokine (C-C motif) ligand 3-like 1
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
HLA-B major histocompatibility complex, class I, B
IFNL3 interferon, lambda 3
IL18 interleukin 18
TGFB1 transforming growth factor, beta 1