Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
BARDET-BIEDL SYNDROME 1, MODIFIER OF
3 0 1 0.14 0 0
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
Tubular basement membrane disintegration
4 0 1 0.12 0 0
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
Thickened superior cerebellar peduncle
4 0 1 0.12 0 0
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
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: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis
6 0 1 1.0E-01 0 0
Multiple small medullary renal cysts
6 0 2 0.22 0 0
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
Thickening of glomerular basement membrane
7 0 1 9.1E-02 0 0
Stage IA Lung Adenocarcinoma AJCC v7
7 0 1 9.1E-02 0 0
Elongated superior cerebellar peduncle
7 0 1 9.1E-02 0 0