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 0.62 0 0
CUI: C1867396
Disease: RADIAL-RENAL SYNDROME
RADIAL-RENAL SYNDROME
6 0 5 0.62 0 0
Benign recurrent intrahepatic cholestasis
10 0 5 0.42 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy
10 0 5 0.42 0 0
CITRULLINEMIA, TYPE II, NEONATAL-ONSET
10 0 5 0.42 0 0
Arthrogryposis with renal dysfunction and cholestasis syndrome
12 0 5 0.36 0 0
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis
15 0 5 0.29 0 0
Arthrogryposis, renal dysfunction, and cholestasis 1
16 0 5 0.28 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency
18 0 5 0.25 0 0
CUI: C1112213
Disease: Cholestasis in newborn
Cholestasis in newborn
19 0 5 0.24 0 0
CUI: C0311361
Disease: Adenomatous goiter
Adenomatous goiter
23 0 5 0.20 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia
26 0 5 0.18 0 0
Progressive intrahepatic cholestasis (disorder)
31 0 5 0.15 0 0
Pancreatic adenocarcinoma metastatic
32 0 5 0.15 0 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice
33 0 5 0.14 0 0
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney
33 0 5 0.14 0 0
CUI: C1332316
Disease: Apocrine breast carcinoma
Apocrine breast carcinoma
1 0 1 0.14 0 0
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome
38 0 5 0.12 0 0
CUI: C1845151
Disease: Glycogen Storage Disease, Type IXD
Glycogen Storage Disease, Type IXD
2 0 1 0.12 0 0
CUI: C1856361
Disease: Doll-like facies
Doll-like facies
2 0 1 0.12 0 0
Cholestasis, progressive familial intrahepatic 1
38 0 5 0.12 0 0
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke
42 0 5 0.11 0 0
CUI: C0031051
Disease: Pericementitis
Pericementitis
3 0 1 0.11 0 0
gamma-Glutamyltransferase deficiency
3 0 1 0.11 0 0
ALCOHOL DEPENDENCE, PROTECTION AGAINST
3 0 1 0.11 0 0