Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F
0.120 GeneticVariation disease BEFREE Congenital stationary night blindess-2 (incomplete congenital stationary night blindness (iCSNB) or CSNB-2) is a nonprogressive, X-linked retinal disease which can lead to clinical symptoms such as myopia, hyperopia, nystagmus, strabismus, decreased visual acuity, and impaired scotopic vision. 17949918 2007
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F
0.120 Biomarker disease BEFREE Clinically, CORDX3 shares some features with CSNB2 but is distinguishable from CSNB2 in that it is progressive, can begin in adulthood, has no nystagmus or hyperopic refraction, has only low grade astigmatism, and in dark adaptation lacks cone threshold and has small or no elevation of rod threshold. 16505158 2006
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F
0.120 Biomarker disease HPO