Disease: Blindness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0456909
Disease: Blindness
Blindness 		0.110 GeneticVariation phenotype BEFREE To determine the progression of cone vision loss in patients with recessive disease from NR2E3 gene mutations. 29971438 2018
CUI: C0456909
Disease: Blindness
Blindness 		0.110 Biomarker phenotype HPO