abnormal pupillary light reflex Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007695
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Genes

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.

Symbol Name
SH3TC2 SH3 domain and tetratricopeptide repeats 2