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: C0240928
Disease: Salt craving
Salt craving 		3 0 2 0.40 0 0
CUI: C0520887
Disease: ST segment depression (finding)
ST segment depression (finding) 		3 0 2 0.40 0 0
CUI: C1969408
Disease: Prominent U wave
Prominent U wave 		3 0 2 0.40 0 0
CUI: C1866500
Disease: Low-to-normal blood pressure
Low-to-normal blood pressure 		4 0 2 0.33 0 0
CUI: C0600125
Disease: Prolonged PR interval
Prolonged PR interval 		5 0 2 0.29 0 0
CUI: C0085570
Disease: Hypokalemic alkalosis
Hypokalemic alkalosis 		10 0 3 0.27 0 0
CUI: C0740898
Disease: Hypokalemic metabolic alkalosis
Hypokalemic metabolic alkalosis 		10 3 3 0.27 3 0.75
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery 		1 0 1 0.25 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney 		1 0 1 0.25 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension 		1 0 1 0.25 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency 		1 0 1 0.25 0 0
CUI: C0268024
Disease: Hyperkalemia, diminished renal excretion
Hyperkalemia, diminished renal excretion 		6 0 2 0.25 0 0
CUI: C0521623
Disease: Kidney crystallization
Kidney crystallization 		1 0 1 0.25 0 0
CUI: C0877138
Disease: Osteopenia periarticular
Osteopenia periarticular 		1 0 1 0.25 0 0
CUI: C1301626
Disease: Hypertension with albuminuria
Hypertension with albuminuria 		1 0 1 0.25 0 0
CUI: C1846348
Disease: Renal potassium wasting
Renal potassium wasting 		6 0 2 0.25 0 0
CUI: C1846349
Disease: Impaired reabsorption of chloride
Impaired reabsorption of chloride 		1 0 1 0.25 0 0
CUI: C2063386
Disease: Left atrial appendage thrombosis
Left atrial appendage thrombosis 		1 0 1 0.25 0 0
CUI: C2902961
Disease: Page kidney
Page kidney 		1 0 1 0.25 0 0
CUI: C4016362
Disease: HYPERPRORENINEMIA, FAMILIAL
HYPERPRORENINEMIA, FAMILIAL 		1 0 1 0.25 0 0
CUI: C4025840
Disease: Abnormal sclera morphology
Abnormal sclera morphology 		1 0 1 0.25 0 0
CUI: C4310923
Disease: BARTTER SYNDROME, TYPE 4B, WITH SENSORINEURAL DEAFNESS
BARTTER SYNDROME, TYPE 4B, WITH SENSORINEURAL DEAFNESS 		1 0 1 0.25 0 0
CUI: C1522135
Disease: Hypermagnesemia result
Hypermagnesemia result 		7 0 2 0.22 0 0
CUI: C4554647
Disease: Hypermagnesemia, CTCAE
Hypermagnesemia, CTCAE 		7 0 2 0.22 0 0
CUI: C0039235
Disease: Tachycardia, Ectopic Junctional
Tachycardia, Ectopic Junctional 		2 0 1 0.20 0 0