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: C2959367
Disease: Nephronophthisis type 4
Nephronophthisis type 4
1 0 1 1.00 0 0
CUI: C1846979
Disease: SENIOR-LOKEN SYNDROME 4
SENIOR-LOKEN SYNDROME 4
2 7 1 0.50 2 9.1E-02
CUI: C1858392
Disease: NEPHRONOPHTHISIS 3
NEPHRONOPHTHISIS 3
6 0 1 0.17 0 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts
8 0 1 0.12 0 0
CUI: C0240595
Disease: Rotary Nystagmus
Rotary Nystagmus
9 0 1 0.11 0 0
CUI: C1855675
Disease: Arima syndrome
Arima syndrome
11 0 1 9.1E-02 0 0
CUI: C1865872
Disease: NEPHRONOPHTHISIS 2
NEPHRONOPHTHISIS 2
14 0 1 7.1E-02 0 0
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile
17 0 1 5.9E-02 0 0
CUI: C1858395
Disease: Tubular atrophy
Tubular atrophy
17 0 1 5.9E-02 0 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment
17 0 1 5.9E-02 0 0
Renal dysplasia and retinal aplasia (disorder)
20 0 1 5.0E-02 0 0
CUI: C4021657
Disease: Abnormality of bone mineral density
Abnormality of bone mineral density
22 0 1 4.5E-02 0 0
CUI: C0020258
Disease: Hydrocephalus, Normal Pressure
Hydrocephalus, Normal Pressure
44 0 1 2.3E-02 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis
49 0 1 2.0E-02 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus
55 0 1 1.8E-02 0 0
CUI: C0085602
Disease: Polydipsia
Polydipsia
61 0 1 1.6E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital
63 0 1 1.6E-02 0 0
CUI: C0032617
Disease: Polyuria
Polyuria
73 0 1 1.4E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss
77 0 1 1.3E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
85 0 1 1.2E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 1 1.1E-02 0 0
CUI: C0687120
Disease: Nephronophthisis
Nephronophthisis
96 103 1 1.0E-02 2 1.7E-02
CUI: C0021359
Disease: Infertility
Infertility
130 5 1 7.7E-03 1 4.8E-02
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 5.2E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.7E-03 0 0