Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0456909
Disease: Blindness
Blindness
0.110 Biomarker phenotype BEFREE Mutations linked to retinitis pigmentosa (RP), a disease that causes blindness in humans, map to the Brr2 regulatory region of Prp8. 26968627 2016
CUI: C0456909
Disease: Blindness
Blindness
0.110 Biomarker phenotype HPO