Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Medullary Cystic Kidney Disease Type 2
5 5 5 0.83 3 0.15
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease
11 2 5 0.42 1 5.3E-02
CUI: C1868139
Disease: Medullary cystic kidney disease 1
Medullary cystic kidney disease 1
5 0 3 0.38 0 0
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3
2 0 2 0.33 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease
3 0 2 0.29 0 0
CUI: C2939174
Disease: Medullary cystic disease
Medullary cystic disease
9 0 3 0.25 0 0
CUI: C0271858
Disease: Tertiary hyperparathyroidism
Tertiary hyperparathyroidism
5 0 2 0.22 0 0
CUI: C3665382
Disease: 2,8-Dihydroxyadenine Urolithiasis
2,8-Dihydroxyadenine Urolithiasis
6 0 2 0.20 0 0
Autosomal dominant tubulointerstitial kidney disease
13 3 3 0.19 1 5.0E-02
CUI: C0268104
Disease: Disorder of purine metabolism
Disorder of purine metabolism
7 0 2 0.18 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens
1 0 1 0.17 0 0
CUI: C1306162
Disease: Kidney replacement disorder
Kidney replacement disorder
1 0 1 0.17 0 0
CUI: C1334425
Disease: Low Grade Malignant Neoplasm
Low Grade Malignant Neoplasm
1 0 1 0.17 0 0
Bilateral Multicystic Dysplastic Kidneys
1 0 1 0.17 0 0
PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)
1 0 1 0.17 0 0
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria
1 2 1 0.17 1 5.3E-02
Bartter syndrome, antenatal , type 2
1 0 1 0.17 0 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts
8 0 2 0.17 0 0
CUI: C1969371
Disease: Impaired renal uric acid clearance
Impaired renal uric acid clearance
1 0 1 0.17 0 0
CUI: C3805186
Disease: Pulmonary leukostasis
Pulmonary leukostasis
1 0 1 0.17 0 0
Abnormality of alkaline phosphatase activity
1 0 1 0.17 0 0
CUI: C4025730
Disease: Renal cortical atrophy
Renal cortical atrophy
1 0 1 0.17 0 0
CUI: C4518822
Disease: 17q12 microdeletion syndrome
17q12 microdeletion syndrome
1 0 1 0.17 0 0
CUI: C0035460
Disease: Rhinitis, Vasomotor
Rhinitis, Vasomotor
2 0 1 0.14 0 0
CUI: C0041323
Disease: Tuberculosis, Oral
Tuberculosis, Oral
2 0 1 0.14 0 0