hemorrhage of the eye Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Bleeding from vessels of the various tissues of the eye. (Human Phenotype Ontology, HP_0011885)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011885
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12 genes associated with the hemorrhage of the eye 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
ATOH7 atonal homolog 7 (Drosophila)
BEST1 bestrophin 1
CAPN5 calpain 5
COL4A1 collagen, type IV, alpha 1
DNM2 dynamin 2
FZD4 frizzled class receptor 4
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
LRP5 low density lipoprotein receptor-related protein 5
PROC protein C (inactivator of coagulation factors Va and VIIIa)
RB1 retinoblastoma 1
TREX1 three prime repair exonuclease 1