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: C2673760
Disease: DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB6 (disorder) 		3 0 3 0.23 0 0
CUI: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) 		4 0 3 0.21 0 0
CUI: C2673761
Disease: DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB3 (disorder) 		4 0 3 0.21 0 0
CUI: C3665333
Disease: Keratitis-Ichthyosis-Deafness Syndrome
Keratitis-Ichthyosis-Deafness Syndrome 		5 0 3 0.20 0 0
CUI: C4021633
Disease: Patchy palmoplantar keratoderma
Patchy palmoplantar keratoderma 		5 0 3 0.20 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss 		22 0 5 0.17 0 0
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b 		2 0 2 0.15 0 0
CUI: C0432330
Disease: Erythrokeratoderma
Erythrokeratoderma 		10 0 3 0.15 0 0
CUI: C4551486
Disease: ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1
ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1 		3 0 2 0.14 0 0
CUI: C0265336
Disease: Senter syndrome
Senter syndrome 		4 0 2 0.13 0 0
CUI: C0395973
Disease: Recessive sensorineural hearing loss
Recessive sensorineural hearing loss 		4 0 2 0.13 0 0
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 0 2 0.13 0 0
CUI: C1832425
Disease: Deafness, Autosomal Dominant 9
Deafness, Autosomal Dominant 9 		4 0 2 0.13 0 0
CUI: C1844678
Disease: Progressive hearing loss stapes fixation
Progressive hearing loss stapes fixation 		4 0 2 0.13 0 0
CUI: C1861326
Disease: Stapes ankylosis
Stapes ankylosis 		4 0 2 0.13 0 0
CUI: C0265961
Disease: Erythrokeratodermia variabilis
Erythrokeratodermia variabilis 		13 0 3 0.13 0 0
CUI: C1848639
Disease: USHER SYNDROME, TYPE IA, FORMERLY
USHER SYNDROME, TYPE IA, FORMERLY 		5 0 2 0.12 0 0
CUI: C1848640
Disease: USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY
USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY 		5 0 2 0.12 0 0
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		15 0 3 0.12 0 0
CUI: C0033074
Disease: Presbycusis
Presbycusis 		6 0 2 0.12 0 0
CUI: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss 		6 0 2 0.12 0 0
CUI: C1866095
Disease: Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 13 		6 0 2 0.12 0 0
CUI: C4021630
Disease: Broad long bones
Broad long bones 		6 0 2 0.12 0 0
CUI: C1969913
Disease: Generalized hyperkeratosis
Generalized hyperkeratosis 		16 0 3 0.12 0 0
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 0 2 0.11 0 0