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 http://compbio.charite.de/hpoweb/showterm?id=HP:0011502
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Genes

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)