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: C0238157
Disease: Benign hematuria
Benign hematuria 		2 0 2 1.00 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 2 0.67 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 2 0.67 0 0
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 2 0.67 0 0
CUI: C3276821
Disease: Thin glomerular basement membrane
Thin glomerular basement membrane 		3 0 2 0.67 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 2 0.67 0 0
CUI: C4746547
Disease: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT 		3 0 2 0.67 0 0
CUI: C4746745
Disease: ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE 		4 0 2 0.50 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 2 0.40 0 0
CUI: C2931861
Disease: Hemorrhagic hereditary nephritis
Hemorrhagic hereditary nephritis 		2 0 1 0.33 0 0
CUI: C0445347
Disease: Thickening of glomerular basement membrane
Thickening of glomerular basement membrane 		7 0 2 0.29 0 0
CUI: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 2 0.25 0 0
CUI: C0027706
Disease: Hereditary nephritis
Hereditary nephritis 		9 0 2 0.22 0 0
CUI: C0154856
Disease: Retinal lattice degeneration
Retinal lattice degeneration 		4 0 1 0.20 0 0
CUI: C4021775
Disease: High-frequency sensorineural hearing impairment
High-frequency sensorineural hearing impairment 		4 0 1 0.20 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 0 2 0.18 0 0
CUI: C4020705
Disease: Glomerulocystic kidney disease
Glomerulocystic kidney disease 		11 0 2 0.18 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 0 2 0.17 0 0
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 0 2 0.15 0 0
CUI: C0239119
Disease: Lenticonus
Lenticonus 		6 0 1 0.14 0 0
CUI: C0544008
Disease: Chandler syndrome
Chandler syndrome 		6 0 1 0.14 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 1 0.12 0 0
CUI: C0242528
Disease: Azotemia
Azotemia 		9 0 1 1.0E-01 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 0 2 1.0E-01 0 0
CUI: C0473237
Disease: Frank hematuria
Frank hematuria 		9 0 1 1.0E-01 0 0