Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 6 8.6E-02 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 63 6 7.9E-02 1 1.1E-02
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		6 106 4 6.9E-02 3 2.3E-02
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		25 0 5 6.6E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 5 6.6E-02 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 5 6.5E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 109 8 6.1E-02 2 1.5E-02
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 4 6.1E-02 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 12 5.9E-02 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 0 4 5.9E-02 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 227 15 5.8E-02 6 2.4E-02
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 12 5.7E-02 0 0
CUI: C0151811
Disease: Subcutaneous nodule
Subcutaneous nodule 		80 0 7 5.4E-02 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		81 0 7 5.4E-02 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 10 5.3E-02 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 5 5.3E-02 0 0
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		24 0 4 5.3E-02 0 0
CUI: C0268654
Disease: Iminoglycinuria
Iminoglycinuria 		4 0 3 5.3E-02 0 0
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 0 3 5.3E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 5 5.2E-02 0 0
CUI: C0155017
Disease: Color Blindness, Blue
Color Blindness, Blue 		25 0 4 5.2E-02 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 53 7 5.2E-02 1 1.2E-02
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 10 10 5.2E-02 1 2.6E-02
CUI: C0155018
Disease: Color Blindness, Acquired
Color Blindness, Acquired 		5 0 3 5.2E-02 0 0
CUI: C0234629
Disease: Abnormal color vision
Abnormal color vision 		5 0 3 5.2E-02 0 0