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: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 0 1 0.50 0 0
CUI: C1863655
Disease: Deafness, Autosomal Recessive 21
Deafness, Autosomal Recessive 21 		1 0 1 0.50 0 0
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 0.50 0 0
CUI: C4023340
Disease: Childhood onset sensorineural hearing impairment
Childhood onset sensorineural hearing impairment 		1 0 1 0.50 0 0
CUI: C1866095
Disease: Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 13 		6 0 2 0.33 0 0
CUI: C4022757
Disease: Moderate hearing impairment
Moderate hearing impairment 		2 0 1 0.33 0 0
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function 		2 0 1 0.33 0 0
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 0 2 0.29 0 0
CUI: C1832476
Disease: Deafness, Autosomal Dominant 10
Deafness, Autosomal Dominant 10 		3 0 1 0.25 0 0
CUI: C0395973
Disease: Recessive sensorineural hearing loss
Recessive sensorineural hearing loss 		4 0 1 0.20 0 0
CUI: C1832425
Disease: Deafness, Autosomal Dominant 9
Deafness, Autosomal Dominant 9 		4 0 1 0.20 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 1 0.17 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 1 0.17 0 0
CUI: C4022758
Disease: Mild hearing impairment
Mild hearing impairment 		6 0 1 0.14 0 0
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		15 0 2 0.13 0 0
CUI: C4021535
Disease: Infantile sensorineural hearing impairment
Infantile sensorineural hearing impairment 		7 4 1 0.12 1 4.3E-02
CUI: C0339534
Disease: Usher syndrome type 2
Usher syndrome type 2 		8 0 1 0.11 0 0
CUI: C2931206
Disease: Usher syndrome, type 1B
Usher syndrome, type 1B 		8 0 1 0.11 0 0
CUI: C4021534
Disease: Adult onset sensorineural hearing impairment
Adult onset sensorineural hearing impairment 		8 2 1 0.11 1 4.8E-02
CUI: C0271215
Disease: Blindness, Legal
Blindness, Legal 		10 0 1 9.1E-02 0 0
CUI: C0206586
Disease: Endolymphatic Hydrops
Endolymphatic Hydrops 		11 0 1 8.3E-02 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 1 8.3E-02 0 0
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 1 8.3E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 1 7.7E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 1 7.1E-02 0 0