Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 778
Gene Symbol: CACNA1F
CACNA1F
CUI: C0038379
Disease: Strabismus
Strabismus
0.110 GeneticVariation 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
CUI: C0038379
Disease: Strabismus
Strabismus
0.110 Biomarker HPO