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: C3281046
Disease: RETINITIS PIGMENTOSA 64
RETINITIS PIGMENTOSA 64 		2 4 2 1.00 1 0.14
CUI: C4319932
Disease: BARDET-BIEDL SYNDROME 21
BARDET-BIEDL SYNDROME 21 		2 2 2 1.00 1 0.20
CUI: C4072973
Disease: Reduced amplitude of dark-adapted bright flash electroretinogram a-wave
Reduced amplitude of dark-adapted bright flash electroretinogram a-wave 		1 0 1 0.50 0 0
CUI: C4476614
Disease: Beaten bronze macular sheen
Beaten bronze macular sheen 		1 0 1 0.50 0 0
CUI: C4049066
Disease: Retinal dystrophy with early macular involvement
Retinal dystrophy with early macular involvement 		2 0 1 0.33 0 0
CUI: C4073101
Disease: Hyperautofluorescent macular lesion
Hyperautofluorescent macular lesion 		4 0 1 0.20 0 0
CUI: C3549703
Disease: Retinal thinning
Retinal thinning 		11 0 1 8.3E-02 0 0
CUI: C4703439
Disease: Abnormality of fundus pigmentation
Abnormality of fundus pigmentation 		14 0 1 6.7E-02 0 0
CUI: C4022792
Disease: Reduced ejection fraction
Reduced ejection fraction 		18 0 1 5.3E-02 0 0
CUI: C1833929
Disease: THYROID CARCINOMA, SPORADIC MEDULLARY
THYROID CARCINOMA, SPORADIC MEDULLARY 		22 0 1 4.3E-02 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change 		24 0 1 4.0E-02 0 0
CUI: C0521694
Disease: Atrophic retina
Atrophic retina 		24 0 1 4.0E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 1 3.8E-02 0 0
CUI: C0497406
Disease: Overweight
Overweight 		27 0 1 3.6E-02 0 0
CUI: C1844562
Disease: Medial flaring of the eyebrow
Medial flaring of the eyebrow 		28 0 1 3.4E-02 0 0
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1 		32 0 1 3.0E-02 0 0
CUI: C0018810
Disease: heart rate
heart rate 		36 0 1 2.7E-02 0 0
CUI: C1288283
Disease: Atrophoderma maculatum
Atrophoderma maculatum 		39 0 1 2.5E-02 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 2.4E-02 0 0
CUI: C0685840
Disease: Congenital hypoplasia of ovary
Congenital hypoplasia of ovary 		44 0 1 2.2E-02 0 0
CUI: C0221353
Disease: Horseshoe Kidney
Horseshoe Kidney 		51 0 1 1.9E-02 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.7E-02 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		61 0 1 1.6E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss 		77 0 1 1.3E-02 0 0
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 		86 0 1 1.1E-02 0 0