Disease: Dyschromatopsia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dyschromatopsia
CUI: C0858618
Disease: Dyschromatopsia
0.010 GeneticVariation BEFREE With regards to p.(Met390Arg) cases, homozygotes showed a relatively more severe ocular phenotype than compound heterozygotes, since more severe fundus alterations and higher frequency of cataracts and dyschromatopsia (not previously described) were documented in the first group. 26082521 2015