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: C1706410
Disease: Atopic IgE-mediated allergic disorder
Atopic IgE-mediated allergic disorder 		3 0 1 0.17 0 0
CUI: C3275929
Disease: Superior semicircular canal dehiscence syndrome
Superior semicircular canal dehiscence syndrome 		3 0 1 0.17 0 0
CUI: C3276419
Disease: USHER SYNDROME, TYPE ID/F, DIGENIC
USHER SYNDROME, TYPE ID/F, DIGENIC 		3 0 1 0.17 0 0
CUI: C0854021
Disease: Abnormal visual field test
Abnormal visual field test 		4 0 1 0.14 0 0
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 57 1 0.14 1 2.7E-03
CUI: C1864871
Disease: Chromosome 17q21.31 Deletion Syndrome
Chromosome 17q21.31 Deletion Syndrome 		4 0 1 0.14 0 0
CUI: C2931208
Disease: Usher syndrome, type 1D
Usher syndrome, type 1D 		4 0 1 0.14 0 0
CUI: C4022676
Disease: Decreased female libido
Decreased female libido 		4 0 1 0.14 0 0
CUI: C4023401
Disease: Abnormality of hair density
Abnormality of hair density 		4 0 1 0.14 0 0
CUI: C0339693
Disease: Internal Ophthalmoplegia
Internal Ophthalmoplegia 		5 0 1 0.12 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 0 3 0.12 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 1 0.12 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 1 0.12 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 2 0.12 0 0
CUI: C4072828
Disease: Sudden loss of visual acuity
Sudden loss of visual acuity 		5 0 1 0.12 0 0
CUI: C4072867
Disease: obsolete Peripheral retinopathy
obsolete Peripheral retinopathy 		5 5 1 0.12 1 3.1E-03
CUI: C0033074
Disease: Presbycusis
Presbycusis 		6 0 1 0.11 0 0
CUI: C3665358
Disease: Galactorrhea
Galactorrhea 		6 0 1 0.11 0 0
CUI: C4020900
Disease: Abnormality of the upper limb
Abnormality of the upper limb 		6 4 1 0.11 1 3.2E-03
CUI: C4023211
Disease: Adrenocorticotropin deficient adrenal insufficiency
Adrenocorticotropin deficient adrenal insufficiency 		6 0 1 0.11 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 4 0.11 0 0
CUI: C0422943
Disease: Visual symptoms
Visual symptoms 		17 0 2 0.11 0 0
CUI: C4021806
Disease: Prelingual sensorineural hearing impairment
Prelingual sensorineural hearing impairment 		17 7 2 0.11 4 1.3E-02
CUI: C4255193
Disease: Bilateral Vestibulopathy
Bilateral Vestibulopathy 		7 0 1 1.0E-01 0 0
CUI: C4551957
Disease: Epilepsy, Familial Temporal Lobe 1
Epilepsy, Familial Temporal Lobe 1 		7 0 1 1.0E-01 0 0