peters anomaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of anterior segment dysgenesis in which abnormal cleavage of the anterior chamber occurs. Peters anomaly is characterized by central, paracentral, or complete corneal opacity. (Human Phenotype Ontology, HP_0000659)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000659
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Genes

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

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
ISPD isoprenoid synthase domain containing
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
Funding