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: C1846242
Disease: Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 		4 0 3 0.19 0 0
CUI: C0241908
Disease: Hematuria, Benign Familial
Hematuria, Benign Familial 		11 0 3 0.13 0 0
CUI: C0344262
Disease: Anterior lenticonus
Anterior lenticonus 		3 0 2 0.12 0 0
CUI: C0403440
Disease: Thin basement membrane disease
Thin basement membrane disease 		12 0 3 0.12 0 0
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found 		12 0 3 0.12 0 0
CUI: C1739392
Disease: Thin glomerular basement membrane disease
Thin glomerular basement membrane disease 		3 0 2 0.12 0 0
CUI: C3278307
Disease: Diffuse glomerular basement membrane lamellation
Diffuse glomerular basement membrane lamellation 		3 0 2 0.12 0 0
CUI: C4746547
Disease: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT 		3 43 2 0.12 1 2.2E-02
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		23 0 4 0.12 0 0
CUI: C1839606
Disease: Low-molecular-weight proteinuria
Low-molecular-weight proteinuria 		4 0 2 0.12 0 0
CUI: C4021775
Disease: High-frequency sensorineural hearing impairment
High-frequency sensorineural hearing impairment 		4 0 2 0.12 0 0
CUI: C4746745
Disease: ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE 		4 0 2 0.12 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		84 0 10 0.11 0 0
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant 		5 0 2 0.11 0 0
CUI: C0239119
Disease: Lenticonus
Lenticonus 		6 1 2 0.11 1 0.25
CUI: C0445347
Disease: Thickening of glomerular basement membrane
Thickening of glomerular basement membrane 		7 0 2 1.0E-01 0 0
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		51 314 6 1.0E-01 2 6.3E-03
CUI: C1567744
Disease: Alport Syndrome, Autosomal Recessive
Alport Syndrome, Autosomal Recessive 		8 0 2 9.5E-02 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 0 3 9.4E-02 0 0
CUI: C0027706
Disease: Hereditary nephritis
Hereditary nephritis 		9 0 2 9.1E-02 0 0
CUI: C0473237
Disease: Frank hematuria
Frank hematuria 		9 1 2 9.1E-02 1 0.25
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary 		23 0 3 8.6E-02 0 0
CUI: C1567742
Disease: Alport Syndrome, X-Linked
Alport Syndrome, X-Linked 		13 0 2 7.7E-02 0 0
CUI: C1857395
Disease: De Toni-Debre-Fanconi Syndrome
De Toni-Debre-Fanconi Syndrome 		14 0 2 7.4E-02 0 0
CUI: C0040457
Disease: Tooth, Supernumerary
Tooth, Supernumerary 		31 0 3 7.0E-02 0 0