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)
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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