retinal calcification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Deposition of calcium salts in the retina. (Human Phenotype Ontology, HP_0007862)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007862
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
FAM111A family with sequence similarity 111, member A
RB1 retinoblastoma 1