Clonorchiasis Gene Set
Dataset
DisGeNET Gene-Disease Associations
Category
disease or phenotype associations
Type
disease
Description
A parasitic helminthiasis infectious disease that involves parasitic infection of the bile ducts of the liver by Clonorchis sinensis. The symptoms include abdominal pain, nausea, diarrhea, and eosinophilia. In long-standing infections, cholangitis, cholelithiasis, pancreatitis, and cholangiocarcinoma can develop. (Human Disease Ontology , DOID_13767 )
External Link
https://www.disgenet.org/browser/0/1/0/C0009021
Similar Terms
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Genes
15 genes associated with the disease Clonorchiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symbol
Name
ACP6
acid phosphatase 6, lysophosphatidic
AK3
adenylate kinase 3
CTSB
cathepsin B
CTSL
cathepsin L
CYP3A5
cytochrome P450, family 3, subfamily A, polypeptide 5
FAS
Fas cell surface death receptor
FASLG
Fas ligand (TNF superfamily, member 6)
FCER2
Fc fragment of IgE, low affinity II, receptor for (CD23)
GOT2
glutamic-oxaloacetic transaminase 2, mitochondrial
NOS2
nitric oxide synthase 2, inducible
PLA2G4A
phospholipase A2, group IVA (cytosolic, calcium-dependent)
PLB1
phospholipase B1
PRDX6
peroxiredoxin 6
TNF
tumor necrosis factor
YWHAE
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon
