|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A conical projection of the posterior surface of the lens, occurring as a developmental anomaly. (Human Phenotype Ontology, HP_0011502)|
|Downloads & Tools|
1 genes associated with the posterior lenticonus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|LAMB2||laminin, beta 2 (laminin S)|