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: C4016750
Disease: GLAUCOMA 1, OPEN ANGLE, A, DIGENIC
GLAUCOMA 1, OPEN ANGLE, A, DIGENIC
2 1 2 0.50 1 2.6E-02
CUI: C1299694
Disease: Glaucomatous visual field defect
Glaucomatous visual field defect
3 0 2 0.40 0 0
CUI: C1856439
Disease: GLAUCOMA 3, PRIMARY CONGENITAL, A
GLAUCOMA 3, PRIMARY CONGENITAL, A
3 34 2 0.40 2 2.9E-02
CUI: C3805911
Disease: Increased cup-to-disc ratio
Increased cup-to-disc ratio
4 0 2 0.33 0 0
Abnormality of cellular immune system
4 3 2 0.33 1 2.5E-02
CUI: C0344299
Disease: Temporal pallor of optic disc
Temporal pallor of optic disc
5 0 2 0.29 0 0
CUI: C4023327
Disease: Central opacification of the cornea
Central opacification of the cornea
5 0 2 0.29 0 0
CUI: C4477011
Disease: Thinning of Descemet membrane
Thinning of Descemet membrane
5 0 2 0.29 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome
1 0 1 0.25 0 0
CUI: C0271342
Disease: Glaucomatous atrophy of optic disc
Glaucomatous atrophy of optic disc
1 1 1 0.25 1 2.6E-02
CUI: C0311237
Disease: Goniodysgenesis
Goniodysgenesis
6 3 2 0.25 1 2.5E-02
Glaucoma due to combination of mechanisms
1 0 1 0.25 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus
1 0 1 0.25 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders
1 0 1 0.25 0 0
CUI: C1856441
Disease: Late onset congenital glaucoma
Late onset congenital glaucoma
1 0 1 0.25 0 0
GLAUCOMA 3, PRIMARY CONGENITAL, A, DIGENIC
1 1 1 0.25 1 2.6E-02
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly
1 0 1 0.25 0 0
CUI: C2931644
Disease: O'Donnell Pappas syndrome
O'Donnell Pappas syndrome
1 0 1 0.25 0 0
GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET
1 0 1 0.25 0 0
CUI: C3640024
Disease: Unilateral microphthalmos
Unilateral microphthalmos
1 0 1 0.25 0 0
CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY
1 0 1 0.25 0 0
CUI: C4016760
Disease: GLAUCOMA, EARLY-ONSET, DIGENIC
GLAUCOMA, EARLY-ONSET, DIGENIC
1 1 1 0.25 1 2.6E-02
CUI: C4017065
Disease: Autosomal dominant keratitis
Autosomal dominant keratitis
1 0 1 0.25 0 0
CUI: C4017066
Disease: ANIRIDIA, ATYPICAL
ANIRIDIA, ATYPICAL
1 0 1 0.25 0 0
CUI: C4017067
Disease: FOVEAL HYPOPLASIA 1 WITH CATARACT
FOVEAL HYPOPLASIA 1 WITH CATARACT
1 0 1 0.25 0 0