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: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss
19 0 1 5.0E-02 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss
22 0 1 4.3E-02 0 0
Hearing Loss, Mixed Conductive-Sensorineural
23 0 1 4.2E-02 0 0
CUI: C1306557
Disease: Chronic venous insufficiency
Chronic venous insufficiency
25 0 1 3.8E-02 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy
25 0 1 3.8E-02 0 0
CUI: C0042076
Disease: Urologic Neoplasms
Urologic Neoplasms
28 0 1 3.4E-02 0 0
CUI: C0342418
Disease: Hypothalamic hamartomas
Hypothalamic hamartomas
29 0 1 3.3E-02 0 0
CUI: C1698196
Disease: Muscle Weakness Upper Limb
Muscle Weakness Upper Limb
29 0 1 3.3E-02 0 0
CUI: C0238651
Disease: Ankle clonus
Ankle clonus
32 0 1 3.0E-02 0 0
CUI: C0032273
Disease: Pneumoconiosis
Pneumoconiosis
33 0 1 2.9E-02 0 0
CUI: C0035067
Disease: Renal Artery Stenosis
Renal Artery Stenosis
37 0 1 2.6E-02 0 0
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy
39 0 1 2.5E-02 0 0
CUI: C0008525
Disease: Choroideremia
Choroideremia
41 0 1 2.4E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
44 0 1 2.2E-02 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1
45 0 1 2.2E-02 0 0
CUI: C0003949
Disease: Asbestosis
Asbestosis
47 0 1 2.1E-02 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
47 0 1 2.1E-02 0 0
CUI: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis
49 0 1 2.0E-02 0 0
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina
49 0 1 2.0E-02 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy
52 0 1 1.9E-02 0 0
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome
52 0 1 1.9E-02 0 0
Dissecting aneurysm of the thoracic aorta
57 0 1 1.7E-02 0 0
CUI: C1260959
Disease: Drusen
Drusen
57 0 1 1.7E-02 0 0
CUI: C1298180
Disease: Single tumor
Single tumor
63 0 1 1.6E-02 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
72 0 1 1.4E-02 0 0