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: C0423421
Disease: Atrophic macular change
Atrophic macular change
24 0 3 5.7E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
44 0 4 5.6E-02 0 0
CUI: C0239119
Disease: Lenticonus
Lenticonus
6 0 2 5.6E-02 0 0
CUI: C0423420
Disease: Absent foveal reflex
Absent foveal reflex
6 0 2 5.6E-02 0 0
CUI: C1262037
Disease: Diabetic cystopathy
Diabetic cystopathy
6 0 2 5.6E-02 0 0
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism
6 0 2 5.6E-02 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
25 0 3 5.6E-02 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis
83 0 6 5.5E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease
45 0 4 5.5E-02 0 0
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
26 0 3 5.5E-02 0 0
CUI: C0007135
Disease: Adenocarcinoma, Scirrhous
Adenocarcinoma, Scirrhous
7 0 2 5.4E-02 0 0
CUI: C2733564
Disease: Full thickness hole of macula lutea
Full thickness hole of macula lutea
7 0 2 5.4E-02 0 0
CUI: C4021563
Disease: Retinal nonattachment
Retinal nonattachment
7 0 2 5.4E-02 0 0
CUI: C4024760
Disease: Progressive visual field defects
Progressive visual field defects
7 0 2 5.4E-02 0 0
CUI: C0026613
Disease: Motor Skills Disorders
Motor Skills Disorders
8 0 2 5.3E-02 0 0
CUI: C0347390
Disease: Skin Papilloma
Skin Papilloma
8 0 2 5.3E-02 0 0
CUI: C0554628
Disease: Group A Streptococcal Infections
Group A Streptococcal Infections
8 0 2 5.3E-02 0 0
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome
9 0 2 5.1E-02 0 0
CUI: C0311338
Disease: Fundus Albipunctatus
Fundus Albipunctatus
9 0 2 5.1E-02 0 0
CUI: C1536148
Disease: Chocolate cyst of ovary
Chocolate cyst of ovary
50 0 4 5.1E-02 0 0
Abnormal subcutaneous fat tissue distribution
9 0 2 5.1E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 12 5.1E-02 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
216 0 12 5.1E-02 0 0
CUI: C0729665
Disease: Arteriovenous graft
Arteriovenous graft
10 0 2 5.0E-02 0 0
CUI: C1865304
Disease: Overfolding of the superior helices
Overfolding of the superior helices
10 0 2 5.0E-02 0 0