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: C4520679
Disease: Abnormal macular morphology
Abnormal macular morphology
0 3 0 0 1 3.0E-02
CUI: C0149771
Disease: Rectocele
Rectocele
1 0 1 2.1E-02 0 0
CUI: C0154870
Disease: Focal chorioretinitis
Focal chorioretinitis
1 0 1 2.1E-02 0 0
CUI: C0267468
Disease: Intussusception of rectum
Intussusception of rectum
1 0 1 2.1E-02 0 0
CUI: C0268072
Disease: Hypercupremia
Hypercupremia
1 0 1 2.1E-02 0 0
CUI: C0271086
Disease: Toxic maculopathy
Toxic maculopathy
1 0 1 2.1E-02 0 0
CUI: C0344297
Disease: Choroidal sclerosis
Choroidal sclerosis
1 0 1 2.1E-02 0 0
CUI: C1300285
Disease: SAUL-WILSON SYNDROME
SAUL-WILSON SYNDROME
1 0 1 2.1E-02 0 0
CUI: C1833564
Disease: CONE-ROD DYSTROPHY 1 (disorder)
CONE-ROD DYSTROPHY 1 (disorder)
1 1 1 2.1E-02 1 3.2E-02
CUI: C1836946
Disease: Peripheral Cone Dystrophy
Peripheral Cone Dystrophy
1 0 1 2.1E-02 0 0
Ulnar-Fibular Ray Defect and Brachydactyly
1 0 1 2.1E-02 0 0
CUI: C1840455
Disease: Mild myopia
Mild myopia
1 0 1 2.1E-02 0 0
CUI: C1841721
Disease: ACHROMATOPSIA 4
ACHROMATOPSIA 4
1 0 1 2.1E-02 0 0
CUI: C1843815
Disease: Newfoundland Rod-Cone Dystrophy
Newfoundland Rod-Cone Dystrophy
1 0 1 2.1E-02 0 0
CUI: C1843816
Disease: Bothnia Retinal Dystrophy
Bothnia Retinal Dystrophy
1 0 1 2.1E-02 0 0
CUI: C1844776
Disease: CONE-ROD DYSTROPHY, X-LINKED, 1
CONE-ROD DYSTROPHY, X-LINKED, 1
1 6 1 2.1E-02 1 2.8E-02
Cataract, Variable Zonular Pulverulent
1 0 1 2.1E-02 0 0
CUI: C1857588
Disease: Amaurosis hypertrichosis
Amaurosis hypertrichosis
1 0 1 2.1E-02 0 0
CUI: C1858386
Disease: Leber Congenital Amaurosis 4
Leber Congenital Amaurosis 4
1 0 1 2.1E-02 0 0
CUI: C1864849
Disease: RETINAL CONE DYSTROPHY 4
RETINAL CONE DYSTROPHY 4
1 0 1 2.1E-02 0 0
CUI: C1864900
Disease: Retinal Cone Dystrophy 3A
Retinal Cone Dystrophy 3A
1 0 1 2.1E-02 0 0
CUI: C1866422
Disease: RETINITIS PIGMENTOSA 19
RETINITIS PIGMENTOSA 19
1 0 1 2.1E-02 0 0
MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO
1 0 1 2.1E-02 0 0
CUI: C2673931
Disease: Hyperthreoninuria
Hyperthreoninuria
1 0 1 2.1E-02 0 0
CUI: C2675185
Disease: Kahrizi Syndrome
Kahrizi Syndrome
1 0 1 2.1E-02 0 0