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: C3838731
Disease: Familial hyperaldosteronism type 1
Familial hyperaldosteronism type 1
6 0 2 0.17 0 0
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia
7 0 2 0.15 0 0
CUI: C0268790
Disease: Renal vascular disorder
Renal vascular disorder
22 0 4 0.15 0 0
CUI: C0020540
Disease: Malignant Hypertension
Malignant Hypertension
23 0 4 0.15 0 0
CUI: C0021313
Disease: Infection of kidney
Infection of kidney
8 0 2 0.14 0 0
CUI: C0042420
Disease: Vasovagal syncope
Vasovagal syncope
16 0 3 0.14 0 0
CUI: C0403622
Disease: Primary vesicoureteric reflux
Primary vesicoureteric reflux
8 0 2 0.14 0 0
CUI: C2062593
Disease: Mesial temporal sclerosis
Mesial temporal sclerosis
8 0 2 0.14 0 0
Congenital posterior urethral valves
26 0 4 0.13 0 0
CUI: C0242528
Disease: Azotemia
Azotemia
9 0 2 0.13 0 0
CUI: C1866956
Disease: Aortic root dilation
Aortic root dilation
9 0 2 0.13 0 0
CUI: C0597048
Disease: Neurogenic hypertension
Neurogenic hypertension
18 0 3 0.13 0 0
Non-ST-segment elevation myocardial infarction (NSTEMI)
18 0 3 0.13 0 0
CUI: C0021295
Disease: Infant, Premature, Diseases
Infant, Premature, Diseases
1 0 1 0.12 0 0
CUI: C0029942
Disease: Overanxious disorder
Overanxious disorder
1 0 1 0.12 0 0
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery
1 0 1 0.12 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney
1 0 1 0.12 0 0
CUI: C0178426
Disease: Oligohydramnios sequence
Oligohydramnios sequence
1 0 1 0.12 0 0
CUI: C0240211
Disease: Lip swelling
Lip swelling
1 0 1 0.12 0 0
CUI: C0263478
Disease: Ophiasis
Ophiasis
1 0 1 0.12 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension
1 0 1 0.12 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency
1 0 1 0.12 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I
1 0 1 0.12 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II
1 0 1 0.12 0 0
CUI: C0342968
Disease: Impaired oxygen delivery
Impaired oxygen delivery
1 0 1 0.12 0 0