Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hypokalemic hypochloremic metabolic alkalosis
3 0 3 0.27 0 0
CUI: C1846351
Disease: Increased urinary potassium
Increased urinary potassium
5 0 3 0.23 0 0
CUI: C1846352
Disease: Hyperchloriduria
Hyperchloriduria
5 0 3 0.23 0 0
CUI: C0085680
Disease: Hypochloremia (disorder)
Hypochloremia (disorder)
7 0 3 0.20 0 0
Serum chloride level decreased (finding)
7 0 3 0.20 0 0
Bartter Syndrome, Type 3, with Hypocalciuria
2 0 2 0.18 0 0
CUI: C1856361
Disease: Doll-like facies
Doll-like facies
2 0 2 0.18 0 0
CUI: C2751312
Disease: BARTTER SYNDROME, TYPE 4B
BARTTER SYNDROME, TYPE 4B
2 0 2 0.18 0 0
BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS
2 0 2 0.18 0 0
CUI: C1865279
Disease: Fetal polyuria
Fetal polyuria
10 0 3 0.17 0 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis
4 0 2 0.15 0 0
CUI: C0348460
Disease: Other hyperaldosteronism
Other hyperaldosteronism
4 0 2 0.15 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
22 0 4 0.14 0 0
CUI: C3671887
Disease: Hypernatriuria
Hypernatriuria
17 0 3 0.12 0 0
Glucose-6-phosphate transport defect
9 0 2 0.11 0 0
CUI: C1846343
Disease: Bartter syndrome, type 3
Bartter syndrome, type 3
9 0 2 0.11 0 0
CUI: C2919796
Disease: Glycogen storage disease type Ia
Glycogen storage disease type Ia
10 0 2 0.11 0 0
CUI: C0042850
Disease: Vitamin B Deficiency
Vitamin B Deficiency
1 0 1 9.1E-02 0 0
CUI: C0598675
Disease: inborn aminoaciduria
inborn aminoaciduria
1 0 1 9.1E-02 0 0
CUI: C0746840
Disease: nephropathy salt wasting
nephropathy salt wasting
1 0 1 9.1E-02 0 0
CUI: C0856208
Disease: Increased serum zinc
Increased serum zinc
1 0 1 9.1E-02 0 0
CUI: C1334425
Disease: Low Grade Malignant Neoplasm
Low Grade Malignant Neoplasm
1 0 1 9.1E-02 0 0
Allergic disorder of respiratory system
1 0 1 9.1E-02 0 0
CUI: C1846349
Disease: Impaired reabsorption of chloride
Impaired reabsorption of chloride
1 0 1 9.1E-02 0 0
CUI: C1865270
Disease: BARTTER SYNDROME, TYPE 4A
BARTTER SYNDROME, TYPE 4A
1 0 1 9.1E-02 0 0