Disease: Night blindness, congenital stationary ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		0.510 Biomarker disease GENOMICS_ENGLAND Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans. 26560832 2016
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		0.510 GeneticVariation disease BEFREE Homozygosity mapping ruled out most known CSNB candidates as well as CACNA2D4 and GNB3. 26368928 2015
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		0.510 GeneticVariation disease ORPHANET Genotyping microarray for CSNB-associated genes. 19578023 2009