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: C1691228
Disease: Cystic Kidney Diseases
Cystic Kidney Diseases
50 0 38 0.38 0 0
CUI: C0311245
Disease: Congenital cystic kidney disease
Congenital cystic kidney disease
31 0 27 0.29 0 0
CUI: C0687120
Disease: Nephronophthisis
Nephronophthisis
96 0 25 0.16 0 0
CUI: C3887499
Disease: Renal cyst
Renal cyst
170 0 35 0.16 0 0
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases
276 0 42 0.13 0 0
CUI: C4552000
Disease: Episodic Kinesigenic Dyskinesia 1
Episodic Kinesigenic Dyskinesia 1
153 0 26 0.12 0 0
CUI: C4277690
Disease: Ciliopathies
Ciliopathies
241 0 34 0.11 0 0
Polycystic Kidney, Autosomal Dominant
280 0 37 0.11 0 0
Autosomal Recessive Polycystic Kidney Disease
69 0 15 0.10 0 0
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
54 0 13 1.0E-01 0 0
CUI: C0334054
Disease: cystic disease
cystic disease
19 0 9 9.1E-02 0 0
CUI: C0268800
Disease: Simple renal cyst
Simple renal cyst
100 0 15 8.6E-02 0 0
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidney
121 0 16 8.2E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital
63 0 11 7.8E-02 0 0
CUI: C3149841
Disease: POLYCYSTIC KIDNEY DISEASE 1
POLYCYSTIC KIDNEY DISEASE 1
39 0 9 7.6E-02 0 0
CUI: C0020258
Disease: Hydrocephalus, Normal Pressure
Hydrocephalus, Normal Pressure
44 0 9 7.3E-02 0 0
CUI: C0030283
Disease: Pancreatic Cyst
Pancreatic Cyst
60 0 10 7.2E-02 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis
49 0 9 7.0E-02 0 0
Renal dysplasia and retinal aplasia (disorder)
20 0 7 6.9E-02 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1
53 0 9 6.8E-02 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 12 6.6E-02 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly
188 0 17 6.5E-02 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers
92 0 11 6.5E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 11 6.4E-02 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly
45 0 8 6.3E-02 0 0