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: C4255088
Disease: Isolated polycystic liver disease
Isolated polycystic liver disease
7 0 1 0.14 0 0
Polycystic Kidney, Type 1 Autosomal Dominant Disease
10 0 1 1.0E-01 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas
13 0 1 7.7E-02 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin
17 0 1 5.9E-02 0 0
CUI: C0267834
Disease: Liver cyst
Liver cyst
26 0 1 3.8E-02 0 0
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease
38 0 1 2.6E-02 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts
46 0 1 2.2E-02 0 0
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
54 0 1 1.9E-02 0 0
Autosomal dominant retinitis pigmentosa
85 0 1 1.2E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 9.7E-03 0 0
CUI: C4552100
Disease: Lynch Syndrome
Lynch Syndrome
103 0 1 9.7E-03 0 0
CUI: C0004604
Disease: Back Pain
Back Pain
110 0 1 9.1E-03 0 0
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage
122 0 1 8.2E-03 0 0
Hereditary Nonpolyposis Colorectal Cancer
174 0 1 5.7E-03 0 0
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases
276 0 1 3.6E-03 0 0
Polycystic Kidney, Autosomal Dominant
280 0 1 3.6E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.3E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 1 3.3E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
315 0 1 3.2E-03 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
446 0 1 2.2E-03 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
523 0 1 1.9E-03 0 0
CUI: C1512409
Disease: Hepatocarcinogenesis
Hepatocarcinogenesis
855 0 1 1.2E-03 0 0
CUI: C0023895
Disease: Liver diseases
Liver diseases
1019 0 1 9.8E-04 0 0