Source: CLINVAR ×
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: C1858677
Disease: LEBER CONGENITAL AMAUROSIS 3 (disorder)
LEBER CONGENITAL AMAUROSIS 3 (disorder) 		0 6 0 0 4 4.3E-02
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		1 0 1 3.6E-02 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		1 0 1 3.6E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		1 0 1 3.6E-02 0 0
CUI: C0339541
Disease: Goldmann-Favre syndrome (disorder)
Goldmann-Favre syndrome (disorder) 		1 0 1 3.6E-02 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		1 0 1 3.6E-02 0 0
CUI: C0423414
Disease: Retinal flecking
Retinal flecking 		1 0 1 3.6E-02 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change 		1 0 1 3.6E-02 0 0
CUI: C0521694
Disease: Atrophic retina
Atrophic retina 		1 0 1 3.6E-02 0 0
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		1 0 1 3.6E-02 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		1 0 1 3.6E-02 0 0
CUI: C1536451
Disease: Central areolar choroidal sclerosis
Central areolar choroidal sclerosis 		1 0 1 3.6E-02 0 0
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration 		1 0 1 3.6E-02 0 0
CUI: C1836517
Disease: Senior-Loken Syndrome 5
Senior-Loken Syndrome 5 		1 11 1 3.6E-02 2 2.0E-02
CUI: C1837713
Disease: JOUBERT SYNDROME 3
JOUBERT SYNDROME 3 		1 0 1 3.6E-02 0 0
CUI: C1837873
Disease: LEBER CONGENITAL AMAUROSIS 9 (disorder)
LEBER CONGENITAL AMAUROSIS 9 (disorder) 		1 10 1 3.6E-02 1 1.0E-02
CUI: C1838603
Disease: Retinitis Pigmentosa 14
Retinitis Pigmentosa 14 		1 0 1 3.6E-02 0 0
CUI: C1838647
Disease: RETINITIS PIGMENTOSA 12 (disorder)
RETINITIS PIGMENTOSA 12 (disorder) 		1 16 1 3.6E-02 5 5.0E-02
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		1 0 1 3.6E-02 0 0
CUI: C1849792
Disease: Achromatopsia 3
Achromatopsia 3 		1 99 1 3.6E-02 3 1.6E-02
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		1 7 1 3.6E-02 1 1.0E-02
CUI: C1857743
Disease: LEBER CONGENITAL AMAUROSIS 12 (disorder)
LEBER CONGENITAL AMAUROSIS 12 (disorder) 		1 5 1 3.6E-02 1 1.1E-02
CUI: C1857779
Disease: SENIOR-LOKEN SYNDROME 6
SENIOR-LOKEN SYNDROME 6 		1 12 1 3.6E-02 2 2.0E-02
CUI: C1857780
Disease: JOUBERT SYNDROME 5
JOUBERT SYNDROME 5 		1 43 1 3.6E-02 5 3.9E-02
CUI: C1857821
Disease: LEBER CONGENITAL AMAUROSIS 10 (disorder)
LEBER CONGENITAL AMAUROSIS 10 (disorder) 		1 17 1 3.6E-02 2 1.9E-02