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: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 6 0.23 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 5 0.21 0 0
CUI: C1863752
Disease: Enlarged Vestibular Aqueduct
Enlarged Vestibular Aqueduct 		4 0 3 0.18 0 0
CUI: C4551715
Disease: Pigmentary retinopathy
Pigmentary retinopathy 		11 0 4 0.17 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 3 0.17 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 3 0.17 0 0
CUI: C1862050
Disease: Cochlear malformation
Cochlear malformation 		5 0 3 0.17 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 5 0.16 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 4 0.15 0 0
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism 		7 0 3 0.15 0 0
CUI: C2676974
Disease: Hypoplasia of the cochlea
Hypoplasia of the cochlea 		7 0 3 0.15 0 0
CUI: C4021806
Disease: Prelingual sensorineural hearing impairment
Prelingual sensorineural hearing impairment 		17 0 4 0.14 0 0
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		10 0 3 0.13 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion 		10 0 3 0.13 0 0
CUI: C1843858
Disease: Atrophy/Degeneration involving the spinal cord
Atrophy/Degeneration involving the spinal cord 		2 0 2 0.12 0 0
CUI: C1868097
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, DIGENIC
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, DIGENIC 		2 0 2 0.12 0 0
CUI: C2931210
Disease: Usher syndrome, type 1F
Usher syndrome, type 1F 		2 0 2 0.12 0 0
CUI: C3150654
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84A
DEAFNESS, AUTOSOMAL RECESSIVE 84A 		2 0 2 0.12 0 0
CUI: C3683791
Disease: Ataxia Neuropathy Spectrum
Ataxia Neuropathy Spectrum 		2 0 2 0.12 0 0
CUI: C4024654
Disease: Postlingual sensorineural hearing impairment
Postlingual sensorineural hearing impairment 		2 0 2 0.12 0 0
CUI: C4531132
Disease: Abnormal morphology of the cerebellar cortex
Abnormal morphology of the cerebellar cortex 		2 0 2 0.12 0 0
CUI: C0155320
Disease: Blindness, Cortical
Blindness, Cortical 		3 0 2 0.12 0 0
CUI: C0270951
Disease: Ocular muscular dystrophy
Ocular muscular dystrophy 		3 0 2 0.12 0 0
CUI: C1843859
Disease: Sensory ataxic neuropathy
Sensory ataxic neuropathy 		3 0 2 0.12 0 0
CUI: C2607947
Disease: Unilateral deafness
Unilateral deafness 		3 0 2 0.12 0 0