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: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B 		8 0 6 0.38 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 5 0.36 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 5 0.36 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 5 0.23 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 5 0.22 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 6 0.20 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 5 0.20 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 5 0.17 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 168 5 0.16 7 4.1E-02
CUI: C1846343
Disease: Bartter syndrome, type 3
Bartter syndrome, type 3 		9 0 3 0.15 0 0
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function 		2 0 2 0.14 0 0
CUI: C3276419
Disease: USHER SYNDROME, TYPE ID/F, DIGENIC
USHER SYNDROME, TYPE ID/F, DIGENIC 		3 0 2 0.13 0 0
CUI: C0085581
Disease: Restrictive lung disease
Restrictive lung disease 		13 0 3 0.12 0 0
CUI: C2931208
Disease: Usher syndrome, type 1D
Usher syndrome, type 1D 		4 0 2 0.12 0 0
CUI: C0398794
Disease: Hypopigmentation-immunodeficiency disease
Hypopigmentation-immunodeficiency disease 		14 0 3 0.12 0 0
CUI: C0730322
Disease: Multiple evanescent white dot syndrome
Multiple evanescent white dot syndrome 		5 0 2 0.12 0 0
CUI: C3888001
Disease: HERMANSKY-PUDLAK SYNDROME 3
HERMANSKY-PUDLAK SYNDROME 3 		5 0 2 0.12 0 0
CUI: C0220724
Disease: CONSTRICTING BANDS, CONGENITAL
CONSTRICTING BANDS, CONGENITAL 		16 0 3 0.11 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 3 0.11 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 5 0.11 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 5 1.0E-01 0 0
CUI: C1832845
Disease: USHER SYNDROME, TYPE ID
USHER SYNDROME, TYPE ID 		8 0 2 1.0E-01 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 5 9.8E-02 0 0
CUI: C4704753
Disease: Urinary Bladder, Underactive
Urinary Bladder, Underactive 		20 0 3 9.7E-02 0 0
CUI: C0205822
Disease: Hibernoma
Hibernoma 		10 0 2 9.1E-02 0 0