Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green
0.120 GeneticVariation disease BEFREE Here, we show that LVAVA haplotype of the OPN1LW gene and MVAVA haplotype of the OPN1MW gene cause apparently nonsyndromic high myopia in young patients but lead to progressive cone-rod dystrophy with deuteranopia and protanopia in middle-aged patients corresponding to a previously unknown disease course. 28358949 2017
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green
0.120 GeneticVariation disease BEFREE We have determined the location of the genes for protan/deutan colorblindness (R/GCP), factor VIII (F8), glucose-6-phosphate dehydrogenase (G6PD), and a series of RFLPs and have derived the following order for this region: R/GCP-GdX-G6PD-F8-DXS115-DXS33-DXS134-D XS15. 2589319 1989
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green
0.120 Biomarker disease HPO