Retinal Fibrosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description invasion of fibrous connective tissue into the retina, often resulting from inflammation or injury (Mammalian Phenotype Ontology, MP_0006186)
External Link https://www.disgenet.org/browser/0/1/0/C1839942
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
CCN2 cellular communication network factor 2
CNTF ciliary neurotrophic factor
TGFB2 transforming growth factor, beta 2