|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of the reflex that controls the diameter of the pupil, in response to the intensity of light that falls on the retina of the eye. (Human Phenotype Ontology, HP_0007695)|
|Downloads & Tools|
1 genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SH3TC2||SH3 domain and tetratricopeptide repeats 2|