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: C1865794
Disease: RHYNS syndrome
RHYNS syndrome 		3 0 1 0.14 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease 		3 0 1 0.14 0 0
CUI: C2675305
Disease: BARDET-BIEDL SYNDROME 1, MODIFIER OF
BARDET-BIEDL SYNDROME 1, MODIFIER OF 		3 0 1 0.14 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 1 0.14 0 0
CUI: C0038604
Disease: Subungual exostoses
Subungual exostoses 		4 0 1 0.12 0 0
CUI: C0086533
Disease: Leiomyoma, Epithelioid
Leiomyoma, Epithelioid 		4 0 1 0.12 0 0
CUI: C1853124
Disease: NEPHROTIC SYNDROME, TYPE 3
NEPHROTIC SYNDROME, TYPE 3 		4 10 1 0.12 1 6.7E-02
CUI: C1857662
Disease: COACH syndrome
COACH syndrome 		4 38 1 0.12 2 4.8E-02
CUI: C1968618
Disease: Tubular basement membrane disintegration
Tubular basement membrane disintegration 		4 0 1 0.12 0 0
CUI: C2673885
Disease: Renal hepatic pancreatic dysplasia Dandy Walker cyst
Renal hepatic pancreatic dysplasia Dandy Walker cyst 		4 0 1 0.12 0 0
CUI: C2931857
Disease: Double cortex
Double cortex 		4 0 1 0.12 0 0
CUI: C4020922
Disease: Enlarged fossa interpeduncularis
Enlarged fossa interpeduncularis 		4 0 1 0.12 0 0
CUI: C4021756
Disease: Thickened superior cerebellar peduncle
Thickened superior cerebellar peduncle 		4 0 1 0.12 0 0
CUI: C4021775
Disease: High-frequency sensorineural hearing impairment
High-frequency sensorineural hearing impairment 		4 0 1 0.12 0 0
CUI: C0271858
Disease: Tertiary hyperparathyroidism
Tertiary hyperparathyroidism 		5 0 1 0.11 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 1 0.11 0 0
CUI: C1859040
Disease: Medullary Cystic Kidney Disease Type 2
Medullary Cystic Kidney Disease Type 2 		5 0 1 0.11 0 0
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1 		5 0 1 0.11 0 0
CUI: C0239119
Disease: Lenticonus
Lenticonus 		6 0 1 1.0E-01 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy 		17 1 2 1.0E-01 1 0.17
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis 		6 0 1 1.0E-01 0 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment 		17 0 2 1.0E-01 0 0
CUI: C4551496
Disease: Hyperuricemic Nephropathy, Familial Juvenile 1
Hyperuricemic Nephropathy, Familial Juvenile 1 		6 18 1 1.0E-01 1 4.3E-02
CUI: C0175692
Disease: Johanson-Blizzard syndrome
Johanson-Blizzard syndrome 		7 0 1 9.1E-02 0 0
CUI: C0268104
Disease: Disorder of purine metabolism
Disorder of purine metabolism 		7 0 1 9.1E-02 0 0