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: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		73 25 9 0.10 1 3.2E-02
CUI: C3266102
Disease: Steroid resistant nephrotic syndrome of childhood
Steroid resistant nephrotic syndrome of childhood 		73 19 9 0.10 1 4.0E-02
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 0 4 0.10 0 0
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome 		23 38 4 9.5E-02 1 2.3E-02
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		37 23 5 9.1E-02 1 3.4E-02
CUI: C4511620
Disease: Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant tubulointerstitial kidney disease 		13 0 3 9.1E-02 0 0
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 2 8.7E-02 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome 		2 0 2 8.7E-02 0 0
CUI: C2931253
Disease: Alport syndrome, dominant type
Alport syndrome, dominant type 		2 0 2 8.7E-02 0 0
CUI: C2931861
Disease: Hemorrhagic hereditary nephritis
Hemorrhagic hereditary nephritis 		2 0 2 8.7E-02 0 0
CUI: C0795949
Disease: Galloway Mowat syndrome
Galloway Mowat syndrome 		15 0 3 8.6E-02 0 0
CUI: C0079301
Disease: Junctional Epidermolysis Bullosa
Junctional Epidermolysis Bullosa 		16 0 3 8.3E-02 0 0
CUI: C0451720
Disease: Nephrotic syndrome, focal and segmental glomerular lesions
Nephrotic syndrome, focal and segmental glomerular lesions 		3 0 2 8.3E-02 0 0
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy 		55 0 6 8.3E-02 0 0
CUI: C2902887
Disease: Nephrotic syndrome with focal and segmental hyalinosis
Nephrotic syndrome with focal and segmental hyalinosis 		3 0 2 8.3E-02 0 0
CUI: C2902888
Disease: Nephrotic syndrome with focal and segmental sclerosis
Nephrotic syndrome with focal and segmental sclerosis 		3 0 2 8.3E-02 0 0
CUI: C2902889
Disease: Nephrotic syndrome with focal glomerulonephritis
Nephrotic syndrome with focal glomerulonephritis 		3 0 2 8.3E-02 0 0
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 2 8.3E-02 0 0
CUI: C3276821
Disease: Thin glomerular basement membrane
Thin glomerular basement membrane 		3 0 2 8.3E-02 0 0
CUI: C4746547
Disease: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT 		3 0 2 8.3E-02 0 0
CUI: C0079297
Disease: Epidermolysis Bullosa Progressiva
Epidermolysis Bullosa Progressiva 		4 0 2 8.0E-02 0 0
CUI: C0478085
Disease: Other epidermolysis bullosa
Other epidermolysis bullosa 		4 0 2 8.0E-02 0 0
CUI: C1710040
Disease: Secondary Focal Segmental Glomerulosclerosis
Secondary Focal Segmental Glomerulosclerosis 		4 0 2 8.0E-02 0 0
CUI: C2673610
Disease: JEB-I
JEB-I 		4 0 2 8.0E-02 0 0
CUI: C4021775
Disease: High-frequency sensorineural hearing impairment
High-frequency sensorineural hearing impairment 		4 0 2 8.0E-02 0 0