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: C0521573
Disease: Coloboma of eyelid
Coloboma of eyelid
4 0 4 1.00 0 0
CUI: C0155299
Disease: Coloboma of optic disc
Coloboma of optic disc
5 0 4 0.80 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris
5 0 4 0.80 0 0
CUI: C1852767
Disease: Hereditary macular coloboma
Hereditary macular coloboma
5 0 4 0.80 0 0
CUI: C4708599
Disease: Coloboma of choroid and retina
Coloboma of choroid and retina
5 0 4 0.80 0 0
CUI: C0029132
Disease: Disorder of the optic nerve
Disorder of the optic nerve
1 0 1 0.25 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome
1 0 1 0.25 0 0
CUI: C0549307
Disease: Morning glory syndrome
Morning glory syndrome
1 0 1 0.25 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders
1 0 1 0.25 0 0
CUI: C1306229
Disease: Dyschromatosis universalis
Dyschromatosis universalis
1 0 1 0.25 0 0
CUI: C1833797
Disease: Optic Nerve Hypoplasia, Bilateral
Optic Nerve Hypoplasia, Bilateral
1 0 1 0.25 0 0
CUI: C1835698
Disease: Keratitis, hereditary
Keratitis, hereditary
1 0 1 0.25 0 0
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak
1 0 1 0.25 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding)
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
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7
1 0 1 0.25 0 0
CUI: C3805604
Disease: FOVEAL HYPOPLASIA 1
FOVEAL HYPOPLASIA 1
1 0 1 0.25 0 0
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
1 0 1 0.25 0 0
COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE
1 0 1 0.25 0 0
CUI: C4554007
Disease: Uveoretinal Coloboma
Uveoretinal Coloboma
7 0 2 0.22 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve
2 0 1 0.20 0 0
CUI: C0431401
Disease: Gillespie syndrome
Gillespie syndrome
2 0 1 0.20 0 0
Congenital ocular coloboma (disorder)
9 0 2 0.18 0 0
CUI: C0011847
Disease: Diabetes
Diabetes
3 0 1 0.17 0 0
CUI: C0206115
Disease: WAGR Syndrome
WAGR Syndrome
3 0 1 0.17 0 0