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: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 317 17 0.33 20 6.2E-02
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy 		39 10 14 0.20 2 6.2E-02
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 59 16 0.20 6 7.8E-02
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina 		49 24 13 0.16 2 4.3E-02
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 10 0.15 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 9 0.15 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 9 0.15 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		44 16 11 0.14 2 5.3E-02
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 53 16 0.14 3 4.1E-02
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 10 0.14 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 10 0.13 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 7 0.13 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 8 0.13 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 8 0.13 0 0
CUI: C1301509
Disease: Severe visual impairment
Severe visual impairment 		35 0 9 0.13 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 14 0.12 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 10 0.12 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 31 13 0.11 1 1.9E-02
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 9 0.11 0 0
CUI: C4025849
Disease: Abnormal foveal morphology
Abnormal foveal morphology 		5 0 5 0.11 0 0
CUI: C4072987
Disease: Yellow/white lesions of the macula
Yellow/white lesions of the macula 		5 0 5 0.11 0 0
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		16 0 6 0.11 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		81 0 12 0.11 0 0
CUI: C0858618
Disease: Dyschromatopsia
Dyschromatopsia 		19 0 6 0.10 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 8 0.10 0 0