Enhanced S-Cone Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis). (Orphanet Rare Disease Ontology, Orphanet_53540)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C564835
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Genes

1 genes/proteins associated with the disease Enhanced S-Cone Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
NR2E3 nuclear receptor subfamily 2, group E, member 3 2.88009