falciform retinal fold Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An area of the retina that is buckled so that a sector-shaped sheet of retina lies in front of the normal retina. This feature is of congenital onset. (Human Phenotype Ontology, HP_0001493)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001493
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Genes

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

Symbol Name
FZD4 frizzled class receptor 4
LRP5 low density lipoprotein receptor-related protein 5
NDP Norrie disease (pseudoglioma)