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: C4016901
Disease: NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO
NEPHROTIC SYNDROME, TYPE 2, SUSCEPTIBILITY TO 		2 0 2 0.29 0 0
CUI: C3825926
Disease: Nephrotic syndrome in children
Nephrotic syndrome in children 		6 1 2 0.18 1 0.14
CUI: C1704320
Disease: Glomerulonephritis, Minimal Change
Glomerulonephritis, Minimal Change 		7 0 2 0.17 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 2 0.17 0 0
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		31 53 5 0.15 2 3.4E-02
CUI: C0268796
Disease: Arteriolar nephrosclerosis
Arteriolar nephrosclerosis 		1 0 1 0.14 0 0
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar 		1 0 1 0.14 0 0
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		1 3 1 0.14 1 0.11
CUI: C1848795
Disease: GRAVES DISEASE, SUSCEPTIBILITY TO, 1
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 		1 1 1 0.14 1 0.14
CUI: C1857692
Disease: Venous varicosities of celiac and mesenteric vessels
Venous varicosities of celiac and mesenteric vessels 		1 0 1 0.14 0 0
CUI: C1860268
Disease: Gonadal tissue inappropriate for external genitalia or chromosomal sex
Gonadal tissue inappropriate for external genitalia or chromosomal sex 		1 0 1 0.14 0 0
CUI: C2675525
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO 		1 5 1 0.14 1 9.1E-02
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		1 9 1 0.14 2 0.14
CUI: C3281084
Disease: Congenital disorder of glycosylation type 1r
Congenital disorder of glycosylation type 1r 		1 0 1 0.14 0 0
CUI: C4025877
Disease: Oral cavity telangiectasia
Oral cavity telangiectasia 		1 0 1 0.14 0 0
CUI: C4225631
Disease: HEREDITARY HEMORRHAGIC TELANGIECTASIA 1
HEREDITARY HEMORRHAGIC TELANGIECTASIA 1 		1 0 1 0.14 0 0
CUI: C4476552
Disease: Dilatation of mesenteric artery
Dilatation of mesenteric artery 		1 0 1 0.14 0 0
CUI: C4477059
Disease: Dilatation of celiac artery
Dilatation of celiac artery 		1 0 1 0.14 0 0
CUI: C0348023
Disease: Spinal arteriovenous malformation
Spinal arteriovenous malformation 		2 0 1 0.12 0 0
CUI: C0403399
Disease: Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome 		11 178 2 0.12 1 5.4E-03
CUI: C0520557
Disease: Arteriovenous malformation of liver
Arteriovenous malformation of liver 		2 0 1 0.12 0 0
CUI: C1619711
Disease: Gastrointestinal telangiectasia
Gastrointestinal telangiectasia 		2 0 1 0.12 0 0
CUI: C1832529
Disease: HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION
HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION 		2 0 1 0.12 0 0
CUI: C1838167
Disease: Nail bed telangiectasia
Nail bed telangiectasia 		2 0 1 0.12 0 0
CUI: C1857693
Disease: Arteriovenous fistulas of celiac and mesenteric vessels
Arteriovenous fistulas of celiac and mesenteric vessels 		2 0 1 0.12 0 0