Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Renal juxtaglomerular cell hypertrophy/hyperplasia
2 0 1 0.50 0 0
CUI: C1866498
Disease: Hyperprostaglandinuria
Hyperprostaglandinuria
2 0 1 0.50 0 0
CUI: C3150358
Disease: Increased serum prostaglandin E2
Increased serum prostaglandin E2
2 0 1 0.50 0 0
CUI: C1866495
Disease: Bartter syndrome, antenatal type 1
Bartter syndrome, antenatal type 1
3 0 1 0.33 0 0
CUI: C0348460
Disease: Other hyperaldosteronism
Other hyperaldosteronism
4 0 1 0.25 0 0
CUI: C1866500
Disease: Low-to-normal blood pressure
Low-to-normal blood pressure
4 0 1 0.25 0 0
CUI: C0232831
Disease: Impairment of urinary concentration
Impairment of urinary concentration
5 0 1 0.20 0 0
CUI: C0268855
Disease: Hypertrophy of bladder
Hypertrophy of bladder
5 0 1 0.20 0 0
CUI: C1846351
Disease: Increased urinary potassium
Increased urinary potassium
5 0 1 0.20 0 0
CUI: C1846352
Disease: Hyperchloriduria
Hyperchloriduria
5 0 1 0.20 0 0
Medullary Cystic Kidney Disease Type 2
5 0 1 0.20 0 0
CUI: C1846348
Disease: Renal potassium wasting
Renal potassium wasting
6 0 1 0.17 0 0
Hyperuricemic Nephropathy, Familial Juvenile 1
6 0 1 0.17 0 0
CUI: C0085680
Disease: Hypochloremia (disorder)
Hypochloremia (disorder)
7 0 1 0.14 0 0
Serum chloride level decreased (finding)
7 0 1 0.14 0 0
CUI: C4525496
Disease: Hamster Insulinoma
Hamster Insulinoma
7 0 1 0.14 0 0
Hyperactive renin-angiotensin system
8 0 1 0.12 0 0
CUI: C1846343
Disease: Bartter syndrome, type 3
Bartter syndrome, type 3
9 0 1 0.11 0 0
CUI: C0085570
Disease: Hypokalemic alkalosis
Hypokalemic alkalosis
10 0 1 1.0E-01 0 0
CUI: C0240783
Disease: Increased circulating renin level
Increased circulating renin level
10 0 1 1.0E-01 0 0
CUI: C0740898
Disease: Hypokalemic metabolic alkalosis
Hypokalemic metabolic alkalosis
10 0 1 1.0E-01 0 0
CUI: C1865279
Disease: Fetal polyuria
Fetal polyuria
10 0 1 1.0E-01 0 0
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease
11 0 1 9.1E-02 0 0
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
15 0 1 6.7E-02 0 0
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria
16 0 1 6.2E-02 0 0