Nephrogenic Systemic Fibrosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Nephrogenic systemic fibrosis (NSF) is a rare systemic fibrosing condition observed in renally impaired patients and characterized by a hardening and thickening of the skin with fibrotic plaques or papules, pruritus, joint pain and stiffness, muscle weakness, limitation of range of motion, and yellowed eyes. It is generally associated with administration of gadolinium-based magnetic resonance imaging contrast agents (GBCA) in patients with kidney disease. (Orphanet Rare Disease Ontology, Orphanet_137617)
External Link https://www.disgenet.org/browser/0/1/0/C3888044
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Genes

12 genes associated with the disease Nephrogenic Systemic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CAV1 caveolin 1, caveolae protein, 22kDa
CCL2 chemokine (C-C motif) ligand 2
CD34 CD34 molecule
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
DCN decorin
EPO erythropoietin
FN1 fibronectin 1
NSF N-ethylmaleimide-sensitive factor
TGFB1 transforming growth factor, beta 1
TLR4 toll-like receptor 4
TLR7 toll-like receptor 7
VCAN versican