posterior lenticonus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A conical projection of the posterior surface of the lens, occurring as a developmental anomaly. (Human Phenotype Ontology, HP_0011502)
External Link
Similar Terms
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.

Symbol Name
LAMB2 laminin, beta 2 (laminin S)