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: C0155299
Disease: Coloboma of optic disc
Coloboma of optic disc
5 0 1 0.17 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris
5 0 1 0.17 0 0
CUI: C1852767
Disease: Hereditary macular coloboma
Hereditary macular coloboma
5 0 1 0.17 0 0
CUI: C4708599
Disease: Coloboma of choroid and retina
Coloboma of choroid and retina
5 0 1 0.17 0 0
CUI: C0003076
Disease: Aniridia
Aniridia
6 0 1 0.14 0 0
Irido-corneo-trabecular dysgenesis (disorder)
7 0 1 0.12 0 0
CUI: C4554007
Disease: Uveoretinal Coloboma
Uveoretinal Coloboma
7 0 1 0.12 0 0
Congenital ocular coloboma (disorder)
9 0 1 1.0E-01 0 0
CUI: C0040427
Disease: Tooth Abnormalities
Tooth Abnormalities
10 0 1 9.1E-02 0 0
CUI: C0265541
Disease: Cranioschisis
Cranioschisis
10 0 1 9.1E-02 0 0
CUI: C0497552
Disease: Congenital neurologic anomalies
Congenital neurologic anomalies
10 0 1 9.1E-02 0 0
CUI: C0524730
Disease: Odontome
Odontome
10 0 1 9.1E-02 0 0
CUI: C0524524
Disease: Pseudoaphakia
Pseudoaphakia
24 0 1 4.0E-02 0 0
CUI: C1510497
Disease: Lens Opacities
Lens Opacities
24 0 1 4.0E-02 0 0
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
32 0 1 3.0E-02 0 0
CUI: C0086543
Disease: Cataract
Cataract
37 0 1 2.6E-02 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies
40 0 1 2.4E-02 0 0
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders
93 0 1 1.1E-02 0 0
CUI: C0002152
Disease: Alloxan Diabetes
Alloxan Diabetes
108 0 1 9.2E-03 0 0
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
108 0 1 9.2E-03 0 0
CUI: C0038433
Disease: Streptozotocin Diabetes
Streptozotocin Diabetes
108 0 1 9.2E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
139 0 1 7.1E-03 0 0
CUI: C0025363
Disease: Mental Retardation, Psychosocial
Mental Retardation, Psychosocial
139 0 1 7.1E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
139 0 1 7.1E-03 0 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
156 0 1 6.4E-03 0 0