Source: ALL
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: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 2 14 0.61 2 1.2E-02
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 9 0.26 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 7 0.24 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 5 0.22 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 5 0.22 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 8 0.22 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 10 0.20 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 74 14 0.18 11 4.8E-02
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 6 0.18 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 5 0.17 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 9 0.16 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 11 5 0.16 7 4.1E-02
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 8 0.14 0 0
CUI: C3276419
Disease: USHER SYNDROME, TYPE ID/F, DIGENIC
USHER SYNDROME, TYPE ID/F, DIGENIC 		3 2 3 0.13 2 1.2E-02
CUI: C1848634
Disease: USHER SYNDROME, TYPE IIA
USHER SYNDROME, TYPE IIA 		4 0 3 0.12 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 4 0.11 0 0
CUI: C0339534
Disease: Usher syndrome type 2
Usher syndrome type 2 		8 0 3 0.11 0 0
CUI: C1832845
Disease: USHER SYNDROME, TYPE ID
USHER SYNDROME, TYPE ID 		8 40 3 0.11 2 9.7E-03
CUI: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B 		8 0 3 0.11 0 0
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 3 9.7E-02 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 8 9.6E-02 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 6 9.4E-02 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		13 24 3 9.1E-02 2 1.1E-02
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function 		2 0 2 8.7E-02 0 0
CUI: C1847089
Disease: USHER SYNDROME, TYPE IG
USHER SYNDROME, TYPE IG 		3 9 2 8.3E-02 2 1.1E-02