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: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 7 0.37 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 7 0.32 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 8 0.31 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 2 4 0.20 1 4.0E-02
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 8 0.19 0 0
CUI: C4022758
Disease: Mild hearing impairment
Mild hearing impairment 		6 4 3 0.19 1 3.7E-02
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 8 0.17 0 0
CUI: C3280041
Disease: RETINITIS PIGMENTOSA 61
RETINITIS PIGMENTOSA 61 		2 2 2 0.15 1 4.0E-02
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 74 10 0.14 1 1.0E-02
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 3 0.14 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		29 41 5 0.14 2 3.2E-02
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 7 0.13 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 2 0.12 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 2 0.12 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 2 3 0.12 2 8.3E-02
CUI: C0339534
Disease: Usher syndrome type 2
Usher syndrome type 2 		8 0 2 0.11 0 0
CUI: C4021534
Disease: Adult onset sensorineural hearing impairment
Adult onset sensorineural hearing impairment 		8 2 2 0.11 1 4.0E-02
CUI: C0271215
Disease: Blindness, Legal
Blindness, Legal 		10 0 2 9.5E-02 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 3 9.4E-02 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 168 3 9.1E-02 2 1.1E-02
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 2 9.1E-02 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 0 2 8.0E-02 0 0
CUI: C3668948
Disease: Circling behavior
Circling behavior 		14 0 2 8.0E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 4 7.8E-02 0 0
CUI: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 0 1 7.7E-02 0 0