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: C2931207
Disease: Usher syndrome, type 1C
Usher syndrome, type 1C 		2 0 1 0.50 0 0
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function 		2 0 1 0.50 0 0
CUI: C1848604
Disease: USHER SYNDROME, TYPE IC
USHER SYNDROME, TYPE IC 		3 36 1 0.33 34 0.85
CUI: C0341305
Disease: Autoimmune enteropathy
Autoimmune enteropathy 		4 0 1 0.25 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 1 0.20 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 1 0.20 0 0
CUI: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B 		8 0 1 0.12 0 0
CUI: C0877104
Disease: Retinal toxicity
Retinal toxicity 		12 0 1 8.3E-02 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 1 7.7E-02 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 0 1 7.1E-02 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 1 7.1E-02 0 0
CUI: C0342288
Disease: Insulin-dependent diabetes mellitus secretory diarrhea syndrome
Insulin-dependent diabetes mellitus secretory diarrhea syndrome 		16 0 1 6.2E-02 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 1 6.2E-02 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 1 4.8E-02 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 1 4.8E-02 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 1 4.5E-02 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 168 1 4.3E-02 5 2.5E-02
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 2.7E-02 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 1 2.4E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 2.4E-02 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 2.1E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 74 1 1.5E-02 3 2.8E-02
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 1 1.5E-02 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		72 0 1 1.4E-02 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.2E-02 0 0