Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60506
Gene Symbol: NYX
NYX
Night Blindness, Congenital Stationary, Type 1A
0.920 CausalMutation CLINVAR

Entrez Id: 60506
Gene Symbol: NYX
NYX
Night blindness, congenital stationary
0.700 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
Night blindness, congenital stationary
0.700 GeneticVariation CLINVAR

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
0.370 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0027092
Disease: Myopia
Myopia
0.130 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0271183
Disease: Severe myopia
Severe myopia
0.130 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0018975
Disease: Hemeralopia
Hemeralopia
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0038379
Disease: Strabismus
Strabismus
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
0.100 Biomarker HPO

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
0.100 GeneticVariation CLINVAR

Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
0.100 Biomarker HPO