Corneal Opacity Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A reduction of corneal clarity. (Human Phenotype Ontology, HP_0007957)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D003318
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Genes

3 genes/proteins associated with the disease Corneal Opacity from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4 2.88009
GLB1 galactosidase, beta 1 2.88009
JAG1 jagged 1 2.88009