retinal hemorrhage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage occurring within the retina. (Human Phenotype Ontology, HP_0000573)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000573
Similar Terms
Downloads & Tools

Genes

5 genes associated with the retinal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
COL4A1 collagen, type IV, alpha 1
DNM2 dynamin 2
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
TREX1 three prime repair exonuclease 1