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: C1866095
Disease: Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 13 		6 0 4 0.67 0 0
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 0 4 0.57 0 0
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		15 0 4 0.27 0 0
CUI: C0948285
Disease: Corneal striae
Corneal striae 		1 2 1 0.25 2 0.20
CUI: C1832475
Disease: Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 11 		1 0 1 0.25 0 0
CUI: C1859116
Disease: Large tarsal bones
Large tarsal bones 		1 0 1 0.25 0 0
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		1 0 1 0.25 0 0
CUI: C1998346
Disease: Autoimmune sensorineural hearing loss
Autoimmune sensorineural hearing loss 		1 0 1 0.25 0 0
CUI: C3281128
Disease: FIBROCHONDROGENESIS 2
FIBROCHONDROGENESIS 2 		1 0 1 0.25 0 0
CUI: C3698167
Disease: Congenital prelingual deafness
Congenital prelingual deafness 		1 0 1 0.25 0 0
CUI: C4021615
Disease: Abnormal metacarpal morphology
Abnormal metacarpal morphology 		1 0 1 0.25 0 0
CUI: C4023340
Disease: Childhood onset sensorineural hearing impairment
Childhood onset sensorineural hearing impairment 		1 0 1 0.25 0 0
CUI: C4025261
Disease: Aplasia/Hypoplasia of the capital femoral epiphysis
Aplasia/Hypoplasia of the capital femoral epiphysis 		1 0 1 0.25 0 0
CUI: C4225261
Disease: SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME
SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME 		1 0 1 0.25 0 0
CUI: C0542259
Disease: Morphological abnormality of the vestibule of the inner ear
Morphological abnormality of the vestibule of the inner ear 		2 0 1 0.20 0 0
CUI: C1832187
Disease: Deafness, Autosomal Dominant 12
Deafness, Autosomal Dominant 12 		2 0 1 0.20 0 0
CUI: C1843895
Disease: Deafness, Autosomal Dominant 44
Deafness, Autosomal Dominant 44 		2 0 1 0.20 0 0
CUI: C1855310
Disease: Megaepiphyseal dwarfism
Megaepiphyseal dwarfism 		2 0 1 0.20 0 0
CUI: C1861481
Disease: Stickler syndrome, type 3
Stickler syndrome, type 3 		2 0 1 0.20 0 0
CUI: C1864746
Disease: Deafness, Autosomal Recessive 53
Deafness, Autosomal Recessive 53 		2 0 1 0.20 0 0
CUI: C2931210
Disease: Usher syndrome, type 1F
Usher syndrome, type 1F 		2 0 1 0.20 0 0
CUI: C4021431
Disease: Abnormality of the vestibulocochlear nerve
Abnormality of the vestibulocochlear nerve 		2 0 1 0.20 0 0
CUI: C4022757
Disease: Moderate hearing impairment
Moderate hearing impairment 		2 0 1 0.20 0 0
CUI: C4024654
Disease: Postlingual sensorineural hearing impairment
Postlingual sensorineural hearing impairment 		2 0 1 0.20 0 0
CUI: C4024656
Disease: Absent vestibular function
Absent vestibular function 		2 0 1 0.20 0 0