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: C0271514
Disease: Low frequency deafness
Low frequency deafness 		15 0 9 5.3E-02 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction 		16 0 9 5.3E-02 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 10 5.3E-02 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 168 9 5.1E-02 2 8.6E-03
CUI: C0152459
Disease: Linear atrophy
Linear atrophy 		149 0 15 5.1E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 13 4.9E-02 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 13 4.9E-02 0 0
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 0 9 4.8E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 15 4.7E-02 0 0
CUI: C0040264
Disease: Tinnitus
Tinnitus 		103 0 12 4.7E-02 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 8 4.7E-02 0 0
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy 		24 20 8 4.5E-02 1 1.2E-02
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 17 4.5E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		96 0 11 4.4E-02 0 0
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 135 7 4.3E-02 1 5.0E-03
CUI: C4023338
Disease: Profound sensorineural hearing impairment
Profound sensorineural hearing impairment 		10 0 7 4.2E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 7 7 4.2E-02 2 2.8E-02
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 7 4.1E-02 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 7 4.1E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 8 4.1E-02 0 0
CUI: C3887873
Disease: Hearing Loss
Hearing Loss 		18 61 7 4.0E-02 3 2.4E-02
CUI: C0018524
Disease: Hallucinations
Hallucinations 		178 0 13 4.0E-02 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 8 4.0E-02 0 0
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		137 0 11 3.8E-02 0 0
CUI: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss 		6 0 6 3.7E-02 0 0