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: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss 		22 0 3 8.6E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 2 7.7E-02 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 12 7.4E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 2 7.4E-02 0 0
CUI: C2732267
Disease: Auditory neuropathy spectrum disorder
Auditory neuropathy spectrum disorder 		28 0 3 7.3E-02 0 0
CUI: C3668948
Disease: Circling behavior
Circling behavior 		14 0 2 7.1E-02 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		29 0 3 7.1E-02 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 12 7.0E-02 0 0
CUI: C1843156
Disease: Progressive sensorineural hearing impairment
Progressive sensorineural hearing impairment 		78 0 6 6.8E-02 0 0
CUI: C0018524
Disease: Hallucinations
Hallucinations 		178 0 12 6.6E-02 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 8 6.5E-02 0 0
CUI: C4021806
Disease: Prelingual sensorineural hearing impairment
Prelingual sensorineural hearing impairment 		17 0 2 6.5E-02 0 0
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		117 30 8 6.4E-02 1 3.3E-02
CUI: C0423431
Disease: Subretinal exudate
Subretinal exudate 		1 0 1 6.2E-02 0 0
CUI: C0685874
Disease: Congenital abnormal shape of inner ear
Congenital abnormal shape of inner ear 		1 0 1 6.2E-02 0 0
CUI: C1300285
Disease: SAUL-WILSON SYNDROME
SAUL-WILSON SYNDROME 		1 1 1 6.2E-02 1 1.00
CUI: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 0 1 6.2E-02 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23 		1 0 1 6.2E-02 0 0
CUI: C1839564
Disease: Jensen syndrome
Jensen syndrome 		1 0 1 6.2E-02 0 0
CUI: C1844579
Disease: Exudative Vitreoretinopathy, Familial, X-Linked Recessive
Exudative Vitreoretinopathy, Familial, X-Linked Recessive 		1 0 1 6.2E-02 0 0
CUI: C1844836
Disease: Ayazi syndrome
Ayazi syndrome 		1 0 1 6.2E-02 0 0
CUI: C1849307
Disease: Increased density of long bones
Increased density of long bones 		1 0 1 6.2E-02 0 0
CUI: C1849309
Disease: Wide distal femoral metaphysis
Wide distal femoral metaphysis 		1 0 1 6.2E-02 0 0
CUI: C1865870
Disease: Deafness, Autosomal Recessive 18
Deafness, Autosomal Recessive 18 		1 0 1 6.2E-02 0 0
CUI: C1865885
Disease: Usher Syndrome, Type IF
Usher Syndrome, Type IF 		1 0 1 6.2E-02 0 0