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: C0235299
Disease: Right upper quadrant pain
Right upper quadrant pain
6 0 5 0.45 0 0
CUI: C1867396
Disease: RADIAL-RENAL SYNDROME
RADIAL-RENAL SYNDROME
6 0 5 0.45 0 0
CUI: C0017927
Disease: Glycogen Storage Disease Type VIII
Glycogen Storage Disease Type VIII
7 0 5 0.42 0 0
Benign recurrent intrahepatic cholestasis
10 0 5 0.33 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy
10 0 5 0.33 0 0
Arthrogryposis with renal dysfunction and cholestasis syndrome
12 0 5 0.29 0 0
CUI: C1112213
Disease: Cholestasis in newborn
Cholestasis in newborn
19 0 6 0.26 0 0
CUI: C1997910
Disease: Citrin deficiency
Citrin deficiency
5 10 3 0.25 6 0.35
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis
15 0 5 0.25 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia
26 0 7 0.24 0 0
Arthrogryposis, renal dysfunction, and cholestasis 1
16 0 5 0.24 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency
18 0 5 0.22 0 0
BCLC Stage A Hepatocellular Carcinoma
2 0 2 0.20 0 0
CUI: C0311361
Disease: Adenomatous goiter
Adenomatous goiter
23 0 5 0.18 0 0
Progressive intrahepatic cholestasis (disorder)
31 0 6 0.17 0 0
Sarcomatoid Hepatocellular Carcinoma
4 0 2 0.17 0 0
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney
33 0 6 0.16 0 0
CUI: C1863844
Disease: Adult-onset citrullinemia type 2
Adult-onset citrullinemia type 2
14 15 3 0.14 8 0.40
CUI: C2349595
Disease: Fetal anemia
Fetal anemia
6 0 2 0.14 0 0
Cholestasis, progressive familial intrahepatic 1
38 0 6 0.14 0 0
Pancreatic adenocarcinoma metastatic
32 0 5 0.14 0 0
CUI: C1266090
Disease: Hepatoid adenocarcinoma
Hepatoid adenocarcinoma
7 0 2 0.13 0 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice
33 0 5 0.13 0 0
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke
42 0 6 0.13 0 0
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome
38 0 5 0.12 0 0