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: 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
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 6.2E-02 0 0
CUI: C3150736
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj 		1 6 1 6.2E-02 1 0.17
CUI: C3152102
Disease: USH1D/F, CDH23/PCDH15, DIGENIC
USH1D/F, CDH23/PCDH15, DIGENIC 		1 0 1 6.2E-02 0 0
CUI: C3275872
Disease: USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC 		1 0 1 6.2E-02 0 0
CUI: C3553944
Disease: USHER SYNDROME, TYPE IJ
USHER SYNDROME, TYPE IJ 		1 0 1 6.2E-02 0 0
CUI: C4015141
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 29
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 		1 0 1 6.2E-02 0 0
CUI: C4016494
Disease: EXUDATIVE VITREORETINOPATHY, X-LINKED
EXUDATIVE VITREORETINOPATHY, X-LINKED 		1 0 1 6.2E-02 0 0
CUI: C4016628
Disease: CEREBELLAR ATAXIA, CATARACT, AND DIABETES MELLITUS
CEREBELLAR ATAXIA, CATARACT, AND DIABETES MELLITUS 		1 0 1 6.2E-02 0 0
CUI: C4021156
Disease: Enlarged semicircular canal
Enlarged semicircular canal 		1 1 1 6.2E-02 1 1.00
CUI: C4021532
Disease: Abnormality of the stapes
Abnormality of the stapes 		1 0 1 6.2E-02 0 0
CUI: C4021549
Disease: Euthyroid hyperthyroxinemia
Euthyroid hyperthyroxinemia 		1 0 1 6.2E-02 0 0
CUI: C4023340
Disease: Childhood onset sensorineural hearing impairment
Childhood onset sensorineural hearing impairment 		1 0 1 6.2E-02 0 0
CUI: C4024758
Disease: Intraretinal exudate
Intraretinal exudate 		1 0 1 6.2E-02 0 0