Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
USHER SYNDROME, TYPE IIA
CUI: C1848634
Disease: USHER SYNDROME, TYPE IIA
0.700 CausalMutation CLINVAR
Congenital sensorineural hearing loss
CUI: C1865866
Disease: Congenital sensorineural hearing loss
0.700 CausalMutation CLINVAR
Usher syndrome type 2
CUI: C0339534
Disease: Usher syndrome type 2
0.700 CausalMutation CLINVAR
Myopia
CUI: C0027092
Disease: Myopia
0.700 CausalMutation CLINVAR
obsolete Rod-cone dystrophy
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
0.700 CausalMutation CLINVAR
Nyctalopia
CUI: C0028077
Disease: Nyctalopia
0.700 CausalMutation CLINVAR