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: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 7 0.50 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 5 0.38 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 9 5 0.25 1 6.2E-02
CUI: C0445347
Disease: Thickening of glomerular basement membrane
Thickening of glomerular basement membrane 		7 0 4 0.25 0 0
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome 		23 38 7 0.24 3 7.0E-02
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 3 0.23 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 3 0.23 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 3 0.23 0 0
CUI: C0027706
Disease: Hereditary nephritis
Hereditary nephritis 		9 0 4 0.22 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 22 4 0.20 1 3.4E-02
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 7 6 0.20 1 7.1E-02
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 3 0.18 0 0
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		37 23 7 0.16 3 0.11
CUI: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 2 0.15 0 0
CUI: C1839884
Disease: Leiomyomatosis, esophageal and vulval, with nephropathy
Leiomyomatosis, esophageal and vulval, with nephropathy 		2 0 2 0.15 0 0
CUI: C2931253
Disease: Alport syndrome, dominant type
Alport syndrome, dominant type 		2 0 2 0.15 0 0
CUI: C2931861
Disease: Hemorrhagic hereditary nephritis
Hemorrhagic hereditary nephritis 		2 0 2 0.15 0 0
CUI: C4024984
Disease: Diffuse leiomyomatosis
Diffuse leiomyomatosis 		2 0 2 0.15 0 0
CUI: C0007775
Disease: Cerebral Atherosclerosis
Cerebral Atherosclerosis 		11 0 3 0.14 0 0
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		51 314 8 0.14 2 6.3E-03
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 2 0.14 0 0
CUI: C3276821
Disease: Thin glomerular basement membrane
Thin glomerular basement membrane 		3 0 2 0.14 0 0
CUI: C4746547
Disease: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT 		3 0 2 0.14 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 0 4 0.14 0 0
CUI: C0086533
Disease: Leiomyoma, Epithelioid
Leiomyoma, Epithelioid 		4 0 2 0.13 0 0