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: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction
13 0 11 0.61 0 0
CUI: C0036454
Disease: Scotoma
Scotoma
21 0 11 0.42 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III
13 0 7 0.32 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY
5 0 5 0.31 0 0
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
5 0 5 0.31 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration
37 0 11 0.26 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A
14 0 6 0.25 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
41 0 11 0.24 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction
16 0 6 0.23 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High
47 0 11 0.21 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder)
14 0 5 0.20 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy
22 0 6 0.19 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I
23 0 6 0.18 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome
68 0 11 0.15 0 0
CUI: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B
8 0 3 0.14 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders
11 0 3 0.12 0 0
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function
2 0 2 0.12 0 0
CUI: C1848604
Disease: USHER SYNDROME, TYPE IC
USHER SYNDROME, TYPE IC
3 0 2 0.12 0 0
CUI: C3276419
Disease: USHER SYNDROME, TYPE ID/F, DIGENIC
USHER SYNDROME, TYPE ID/F, DIGENIC
3 0 2 0.12 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
42 0 6 0.12 0 0
CUI: C2931208
Disease: Usher syndrome, type 1D
Usher syndrome, type 1D
4 0 2 0.11 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 12 0.10 0 0
CUI: C4022758
Disease: Mild hearing impairment
Mild hearing impairment
6 0 2 1.0E-01 0 0
CUI: C2676973
Disease: Dilatated internal auditory canal
Dilatated internal auditory canal
7 2 2 9.5E-02 1 0.50
CUI: C1832845
Disease: USHER SYNDROME, TYPE ID
USHER SYNDROME, TYPE ID
8 0 2 9.1E-02 0 0