abnormal intraocular pressure Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly in the amount of force per unit area exerted by the intraocular fluid within the eye. (Human Phenotype Ontology, HP_0012632)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012632
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4 genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
HMX1 H6 family homeobox 1
LTBP2 latent transforming growth factor beta binding protein 2
PXDN peroxidasin