Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Elongated superior cerebellar peduncle
7 0 2 9.1E-02 0 0
CUI: C0687120
Disease: Nephronophthisis
Nephronophthisis
96 0 9 8.7E-02 0 0
CUI: C0032617
Disease: Polyuria
Polyuria
73 0 7 8.4E-02 0 0
CUI: C0266619
Disease: Potter's facies
Potter's facies
9 0 2 8.3E-02 0 0
CUI: C4021657
Disease: Abnormality of bone mineral density
Abnormality of bone mineral density
22 0 3 8.3E-02 0 0
Decreased glomerular filtration rate
11 0 2 7.7E-02 0 0
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease
11 0 2 7.7E-02 0 0
CUI: C0264733
Disease: Ventricular dilatation (disorder)
Ventricular dilatation (disorder)
13 0 2 7.1E-02 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage
14 0 2 6.9E-02 0 0
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome
15 0 2 6.7E-02 0 0
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital
31 0 3 6.7E-02 0 0
Renal Tubular Transport, Inborn Errors
1 0 1 5.9E-02 0 0
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery
1 0 1 5.9E-02 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney
1 0 1 5.9E-02 0 0
CUI: C0264639
Disease: High-renin essential hypertension
High-renin essential hypertension
1 0 1 5.9E-02 0 0
CUI: C0264693
Disease: Acute coronary insufficiency
Acute coronary insufficiency
1 0 1 5.9E-02 0 0
CUI: C0521623
Disease: Kidney crystallization
Kidney crystallization
1 0 1 5.9E-02 0 0
CUI: C0877138
Disease: Osteopenia periarticular
Osteopenia periarticular
1 0 1 5.9E-02 0 0
CUI: C1301626
Disease: Hypertension with albuminuria
Hypertension with albuminuria
1 0 1 5.9E-02 0 0
CUI: C1306162
Disease: Kidney replacement disorder
Kidney replacement disorder
1 0 1 5.9E-02 0 0
CUI: C1334425
Disease: Low Grade Malignant Neoplasm
Low Grade Malignant Neoplasm
1 0 1 5.9E-02 0 0
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria
1 0 1 5.9E-02 0 0
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
1 0 1 5.9E-02 0 0
CUI: C1847013
Disease: NEPHRONOPHTHISIS 4
NEPHRONOPHTHISIS 4
1 0 1 5.9E-02 0 0
CUI: C1853153
Disease: JOUBERT SYNDROME 6
JOUBERT SYNDROME 6
1 0 1 5.9E-02 0 0