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: C0339534
Disease: Usher syndrome type 2
Usher syndrome type 2 		8 0 1 0.12 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 1 9.1E-02 0 0
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 1 9.1E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 1 8.3E-02 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 1 4.8E-02 0 0
CUI: C0575090
Disease: Equilibration disorder
Equilibration disorder 		22 0 1 4.5E-02 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 1 4.5E-02 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 2.7E-02 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 1 2.6E-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: C0011053
Disease: Deafness
Deafness 		62 0 1 1.6E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 1 1.5E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		96 0 1 1.0E-02 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		109 0 1 9.2E-03 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision 		115 0 1 8.7E-03 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 1 8.6E-03 0 0
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		117 0 1 8.5E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 8.4E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 6.3E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 6.1E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 6.0E-03 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations 		178 0 1 5.6E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 5.2E-03 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 1 4.3E-03 0 0