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: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 0 6 7.6E-02 0 0
CUI: C4021533
Disease: Severe sensorineural hearing impairment
Severe sensorineural hearing impairment 		23 0 6 7.6E-02 0 0
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		10 0 5 7.5E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 5 7.2E-02 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 5 7.1E-02 0 0
CUI: C1691779
Disease: Sensory hearing loss
Sensory hearing loss 		14 0 5 7.0E-02 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 5 7.0E-02 0 0
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		15 0 5 6.9E-02 0 0
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 0 6 6.6E-02 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 6 6.5E-02 0 0
CUI: C0395973
Disease: Recessive sensorineural hearing loss
Recessive sensorineural hearing loss 		4 0 4 6.5E-02 0 0
CUI: C3266898
Disease: Waardenburg Syndrome
Waardenburg Syndrome 		21 0 5 6.4E-02 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 4 6.3E-02 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 4 6.3E-02 0 0
CUI: C0033074
Disease: Presbycusis
Presbycusis 		6 0 4 6.2E-02 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 6 6.2E-02 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 6 6.1E-02 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 6 5.8E-02 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment 		740 0 44 5.8E-02 0 0
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		14 0 4 5.6E-02 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 44 5.5E-02 0 0
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		16 0 4 5.4E-02 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 4 5.4E-02 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		61 0 6 5.1E-02 0 0
CUI: C0040264
Disease: Tinnitus
Tinnitus 		103 0 8 5.1E-02 0 0