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: C1306122
Disease: Oguchi disease
Oguchi disease 		8 0 3 0.33 0 0
CUI: C0344297
Disease: Choroidal sclerosis
Choroidal sclerosis 		1 0 1 0.25 0 0
CUI: C1833564
Disease: CONE-ROD DYSTROPHY 1 (disorder)
CONE-ROD DYSTROPHY 1 (disorder) 		1 0 1 0.25 0 0
CUI: C2673931
Disease: Hyperthreoninuria
Hyperthreoninuria 		1 0 1 0.25 0 0
CUI: C3150678
Disease: OGUCHI DISEASE 2
OGUCHI DISEASE 2 		1 0 1 0.25 0 0
CUI: C4551884
Disease: Choroidal Dystrophy, Central Areolar 1
Choroidal Dystrophy, Central Areolar 1 		1 0 1 0.25 0 0
CUI: C0233593
Disease: Eye poking
Eye poking 		2 0 1 0.20 0 0
CUI: C1848861
Disease: Hyperthreoninemia
Hyperthreoninemia 		2 0 1 0.20 0 0
CUI: C4551824
Disease: Oguchi Disease 1
Oguchi Disease 1 		2 0 1 0.20 0 0
CUI: C1335684
Disease: Rectal Lipoma
Rectal Lipoma 		3 0 1 0.17 0 0
CUI: C1832976
Disease: Cone-Rod Dystrophy 5
Cone-Rod Dystrophy 5 		3 0 1 0.17 0 0
CUI: C1866293
Disease: Retinal cone dystrophy 2
Retinal cone dystrophy 2 		3 0 1 0.17 0 0
CUI: C2673929
Disease: Fundus atrophy
Fundus atrophy 		3 0 1 0.17 0 0
CUI: C3551052
Disease: Night blindness, stationary
Night blindness, stationary 		10 0 2 0.17 0 0
CUI: C4073085
Disease: Foveal photoreceptor outer segment loss on macular OCT
Foveal photoreceptor outer segment loss on macular OCT 		3 0 1 0.17 0 0
CUI: C1852548
Disease: Absent retinal pigment epithelium
Absent retinal pigment epithelium 		4 0 1 0.14 0 0
CUI: C4073101
Disease: Hyperautofluorescent macular lesion
Hyperautofluorescent macular lesion 		4 0 1 0.14 0 0
CUI: C1849394
Disease: Enhanced S-Cone Syndrome
Enhanced S-Cone Syndrome 		14 0 2 0.12 0 0
CUI: C3275758
Disease: Choriocapillaris atrophy
Choriocapillaris atrophy 		5 0 1 0.12 0 0
CUI: C4073099
Disease: Perifoveal ring of hyperautofluorescence
Perifoveal ring of hyperautofluorescence 		5 0 1 0.12 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness 		16 0 2 0.11 0 0
CUI: C0339530
Disease: Progressive cone-rod dystrophy
Progressive cone-rod dystrophy 		6 0 1 0.11 0 0
CUI: C1837873
Disease: LEBER CONGENITAL AMAUROSIS 9 (disorder)
LEBER CONGENITAL AMAUROSIS 9 (disorder) 		6 0 1 0.11 0 0
CUI: C1867326
Disease: RETINAL CONE DYSTROPHY 1
RETINAL CONE DYSTROPHY 1 		6 0 1 0.11 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea 		7 0 1 1.0E-01 0 0