Gene: CACNA1F ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F 		0.110 Biomarker disease HPO
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F 		0.110 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