congenital myopia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Myopia apparent at birth. (Human Phenotype Ontology, HP_0008012)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008012
Similar Terms
Downloads & Tools

Genes

2 genes associated with the congenital myopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)