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: C1849095
Disease: Cochlear degeneration
Cochlear degeneration 		3 0 2 0.18 0 0
CUI: C4551509
Disease: Jervell And Lange-Nielsen Syndrome 1
Jervell And Lange-Nielsen Syndrome 1 		4 0 2 0.17 0 0
CUI: C0403654
Disease: Bladder outflow obstruction
Bladder outflow obstruction 		5 0 2 0.15 0 0
CUI: C2732413
Disease: Postexertional fatigue
Postexertional fatigue 		5 0 2 0.15 0 0
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia 		20 0 3 0.11 0 0
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome 		10 0 2 0.11 0 0
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		11 0 2 0.11 0 0
CUI: C0268016
Disease: Chronic hypokalemia
Chronic hypokalemia 		1 0 1 1.0E-01 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 1.0E-01 0 0
CUI: C0948285
Disease: Corneal striae
Corneal striae 		1 0 1 1.0E-01 0 0
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia 		1 0 1 1.0E-01 0 0
CUI: C1834013
Disease: Odontoma dysphagia syndrome
Odontoma dysphagia syndrome 		1 0 1 1.0E-01 0 0
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		1 0 1 1.0E-01 0 0
CUI: C1838263
Disease: Deafness, Autosomal Recessive 3
Deafness, Autosomal Recessive 3 		1 0 1 1.0E-01 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 1.0E-01 0 0
CUI: C1843738
Disease: LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C1867904
Disease: LONG QT SYNDROME 5
LONG QT SYNDROME 5 		1 0 1 1.0E-01 0 0
CUI: C1970239
Disease: DEAFNESS, AUTOSOMAL RECESSIVE, 24
DEAFNESS, AUTOSOMAL RECESSIVE, 24 		1 0 1 1.0E-01 0 0
CUI: C1998346
Disease: Autoimmune sensorineural hearing loss
Autoimmune sensorineural hearing loss 		1 0 1 1.0E-01 0 0
CUI: C2676723
Disease: JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)
JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C2829265
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 86
DEAFNESS, AUTOSOMAL RECESSIVE 86 		1 0 1 1.0E-01 0 0
CUI: C3150956
Disease: LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 1.0E-01 0 0
CUI: C3553936
Disease: PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) 		1 38 1 1.0E-01 1 2.6E-02
CUI: C3553937
Disease: PEROXISOME BIOGENESIS DISORDER 4B
PEROXISOME BIOGENESIS DISORDER 4B 		1 35 1 1.0E-01 2 5.7E-02
CUI: C3553944
Disease: USHER SYNDROME, TYPE IJ
USHER SYNDROME, TYPE IJ 		1 0 1 1.0E-01 0 0