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: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 59 39 0.75 10 0.17
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 317 12 0.24 2 6.2E-03
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina 		49 24 15 0.21 4 0.13
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 24 14 0.20 2 6.2E-02
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 13 0.18 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 9 0.16 0 0
CUI: C1842914
Disease: Adult-Onset Vitelliform Macular Dystrophy
Adult-Onset Vitelliform Macular Dystrophy 		8 0 6 0.15 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		44 16 10 0.14 2 8.3E-02
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 53 15 0.14 2 3.3E-02
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 9 0.13 0 0
CUI: C1857644
Disease: Retinal pigment epithelial mottling
Retinal pigment epithelial mottling 		16 0 6 0.12 0 0
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		10 0 5 0.11 0 0
CUI: C1536451
Disease: Central areolar choroidal sclerosis
Central areolar choroidal sclerosis 		10 0 5 0.11 0 0
CUI: C3549703
Disease: Retinal thinning
Retinal thinning 		11 0 5 0.11 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 8 0.11 0 0
CUI: C0275911
Disease: Tuberculosis of intestines
Tuberculosis of intestines 		24 0 6 0.11 0 0
CUI: C4048273
Disease: Chorioretinal atrophy
Chorioretinal atrophy 		24 4 6 0.11 1 7.7E-02
CUI: C0375019
Disease: Human T-cell lymphotrophic virus, type I [HTLV-I]
Human T-cell lymphotrophic virus, type I [HTLV-I] 		25 0 6 0.10 0 0
CUI: C1260959
Disease: Drusen
Drusen 		57 18 9 0.10 1 3.7E-02
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		25 0 6 0.10 0 0
CUI: C0339513
Disease: Dominant drusen
Dominant drusen 		4 2 4 0.10 1 9.1E-02
CUI: C1320640
Disease: Peripheral retinal degeneration
Peripheral retinal degeneration 		4 0 4 0.10 0 0
CUI: C1838644
Disease: Stargardt disease 3
Stargardt disease 3 		4 0 4 0.10 0 0
CUI: C4025849
Disease: Abnormal foveal morphology
Abnormal foveal morphology 		5 0 4 1.0E-01 0 0
CUI: C4072987
Disease: Yellow/white lesions of the macula
Yellow/white lesions of the macula 		5 0 4 1.0E-01 0 0