retinal hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage occurring within the retina. (Human Phenotype Ontology, HP_0000573)
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5 gene mutations causing the retinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FZD4 frizzled class receptor 4
IL18 interleukin 18
PDGFRB platelet-derived growth factor receptor, beta polypeptide
TSPAN12 tetraspanin 12
VEGFA vascular endothelial growth factor A