retinal fibrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description invasion of fibrous connective tissue into the retina, often resulting from inflammation or injury (Mammalian Phenotype Ontology, MP_0006186)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006186
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Genes

1 gene mutations causing the retinal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PDGFB platelet-derived growth factor beta polypeptide