sutural cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of congenital cataract in which the opacity follows the anterior or posterior Y suture. (Human Phenotype Ontology, HP_0010695)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010695
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Genes

4 genes associated with the sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CRYBA1 crystallin, beta A1
CRYBB2 crystallin, beta B2
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
SEC23A Sec23 homolog A (S. cerevisiae)