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: C0339462
Disease: Macular retinoschisis
Macular retinoschisis 		0 1 0 0 1 4.8E-02
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		0 9 0 0 1 3.4E-02
CUI: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement 		1 0 1 7.1E-02 0 0
CUI: C0339541
Disease: Goldmann-Favre syndrome (disorder)
Goldmann-Favre syndrome (disorder) 		1 2 1 7.1E-02 1 4.5E-02
CUI: C1744705
Disease: Atrophy of optic disc
Atrophy of optic disc 		1 0 1 7.1E-02 0 0
CUI: C1834330
Disease: Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type
Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type 		1 0 1 7.1E-02 0 0
CUI: C1845407
Disease: CONE-ROD DYSTROPHY, X-LINKED, 3
CONE-ROD DYSTROPHY, X-LINKED, 3 		1 0 1 7.1E-02 0 0
CUI: C1970163
Disease: RETINITIS PIGMENTOSA 37 (disorder)
RETINITIS PIGMENTOSA 37 (disorder) 		1 6 1 7.1E-02 3 0.12
CUI: C2932677
Disease: Idiopathic Juxtafoveal Retinal Telangiectasia
Idiopathic Juxtafoveal Retinal Telangiectasia 		1 0 1 7.1E-02 0 0
CUI: C3150678
Disease: OGUCHI DISEASE 2
OGUCHI DISEASE 2 		1 0 1 7.1E-02 0 0
CUI: C3151086
Disease: Retinitis Pigmentosa 20
Retinitis Pigmentosa 20 		1 0 1 7.1E-02 0 0
CUI: C4016457
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE 		1 0 1 7.1E-02 0 0
CUI: C4072868
Disease: Paravenous chorioretinal atrophy
Paravenous chorioretinal atrophy 		1 0 1 7.1E-02 0 0
CUI: C4072995
Disease: Difficulty adjusting from light to dark
Difficulty adjusting from light to dark 		1 0 1 7.1E-02 0 0
CUI: C4274354
Disease: Severe early childhood onset retinal dystrophy
Severe early childhood onset retinal dystrophy 		1 0 1 7.1E-02 0 0
CUI: C4707246
Disease: Biallelic RPE65 mutation associated retinal dystrophy
Biallelic RPE65 mutation associated retinal dystrophy 		1 0 1 7.1E-02 0 0
CUI: C0233593
Disease: Eye poking
Eye poking 		2 0 1 6.7E-02 0 0
CUI: C1849397
Disease: Retinoschisis of Fovea
Retinoschisis of Fovea 		2 0 1 6.7E-02 0 0
CUI: C1849821
Disease: Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial 		2 0 1 6.7E-02 0 0
CUI: C1857618
Disease: Achromatopsia 2
Achromatopsia 2 		2 0 2 0.14 0 0
CUI: C1868310
Disease: Pigmented Paravenous Chorioretinal Atrophy
Pigmented Paravenous Chorioretinal Atrophy 		2 0 1 6.7E-02 0 0
CUI: C2931753
Disease: Achromatopsia incomplete, X-linked
Achromatopsia incomplete, X-linked 		2 0 1 6.7E-02 0 0
CUI: C3151202
Disease: LEBER CONGENITAL AMAUROSIS 8
LEBER CONGENITAL AMAUROSIS 8 		2 0 1 6.7E-02 0 0
CUI: C3887937
Disease: CONE DYSTROPHY 5, X-LINKED
CONE DYSTROPHY 5, X-LINKED 		2 0 1 6.7E-02 0 0
CUI: C4024765
Disease: Peripapillary chorioretinal atrophy
Peripapillary chorioretinal atrophy 		2 0 1 6.7E-02 0 0