|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A condition where the retina contains no functional cone cells, so that in addition to the absence of color discrimination, vision in lights of normal intensity is difficult. (Human Phenotype Ontology, HP_0011516)|
|Downloads & Tools|
2 genes associated with the rod monochromacy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.