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: C1969371
Disease: Impaired renal uric acid clearance
Impaired renal uric acid clearance 		1 0 1 5.9E-02 0 0
CUI: C2063386
Disease: Left atrial appendage thrombosis
Left atrial appendage thrombosis 		1 0 1 5.9E-02 0 0
CUI: C2902961
Disease: Page kidney
Page kidney 		1 0 1 5.9E-02 0 0
CUI: C2959367
Disease: Nephronophthisis type 4
Nephronophthisis type 4 		1 0 1 5.9E-02 0 0
CUI: C3150419
Disease: NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1
NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 		1 0 1 5.9E-02 0 0
CUI: C3150796
Disease: NEPHRONOPHTHISIS 11
NEPHRONOPHTHISIS 11 		1 0 1 5.9E-02 0 0
CUI: C3279905
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 		1 0 1 5.9E-02 0 0
CUI: C3280617
Disease: Nephronophthisis-like nephropathy
Nephronophthisis-like nephropathy 		1 0 1 5.9E-02 0 0
CUI: C3553636
Disease: INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL
INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL 		1 0 1 5.9E-02 0 0
CUI: C3554634
Disease: Light complexion
Light complexion 		1 0 1 5.9E-02 0 0
CUI: C3805186
Disease: Pulmonary leukostasis
Pulmonary leukostasis 		1 0 1 5.9E-02 0 0
CUI: C3890591
Disease: NEPHRONOPHTHISIS 18
NEPHRONOPHTHISIS 18 		1 0 1 5.9E-02 0 0
CUI: C4016362
Disease: HYPERPRORENINEMIA, FAMILIAL
HYPERPRORENINEMIA, FAMILIAL 		1 0 1 5.9E-02 0 0
CUI: C4016445
Disease: NEPHROLITHIASIS, X-LINKED RECESSIVE
NEPHROLITHIASIS, X-LINKED RECESSIVE 		1 0 1 5.9E-02 0 0
CUI: C4017203
Disease: BARDET-BIEDL SYNDROME 14, MODIFIER OF
BARDET-BIEDL SYNDROME 14, MODIFIER OF 		1 0 1 5.9E-02 0 0
CUI: C4025730
Disease: Renal cortical atrophy
Renal cortical atrophy 		1 0 1 5.9E-02 0 0
CUI: C4225228
Disease: NEPHROTIC SYNDROME, TYPE 11
NEPHROTIC SYNDROME, TYPE 11 		1 0 1 5.9E-02 0 0
CUI: C4310627
Disease: MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME
MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME 		1 0 1 5.9E-02 0 0
CUI: C4748084
Disease: OVARIAN DYSGENESIS 6
OVARIAN DYSGENESIS 6 		1 0 1 5.9E-02 0 0
CUI: C4748549
Disease: NEPHROTIC SYNDROME, TYPE 18
NEPHROTIC SYNDROME, TYPE 18 		1 0 1 5.9E-02 0 0
CUI: C0543800
Disease: Idiopathic hypercalciuria
Idiopathic hypercalciuria 		20 0 2 5.7E-02 0 0
CUI: C0035460
Disease: Rhinitis, Vasomotor
Rhinitis, Vasomotor 		2 0 1 5.6E-02 0 0
CUI: C0039235
Disease: Tachycardia, Ectopic Junctional
Tachycardia, Ectopic Junctional 		2 0 1 5.6E-02 0 0
CUI: C0041323
Disease: Tuberculosis, Oral
Tuberculosis, Oral 		2 0 1 5.6E-02 0 0
CUI: C0085569
Disease: Metabolic acidosis, NAG, acidifying salts
Metabolic acidosis, NAG, acidifying salts 		2 0 1 5.6E-02 0 0