Source: ALL
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: C0149841
Disease: Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis 		10 0 7 0.39 0 0
CUI: C4551984
Disease: Arthrogryposis with renal dysfunction and cholestasis syndrome
Arthrogryposis with renal dysfunction and cholestasis syndrome 		12 0 7 0.35 0 0
CUI: C0235299
Disease: Right upper quadrant pain
Right upper quadrant pain 		6 0 5 0.31 0 0
CUI: C1867396
Disease: RADIAL-RENAL SYNDROME
RADIAL-RENAL SYNDROME 		6 0 5 0.31 0 0
CUI: C0017927
Disease: Glycogen Storage Disease Type VIII
Glycogen Storage Disease Type VIII 		7 0 5 0.29 0 0
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		16 0 7 0.29 0 0
CUI: C1112213
Disease: Cholestasis in newborn
Cholestasis in newborn 		19 0 7 0.26 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy 		10 0 5 0.25 0 0
CUI: C1853942
Disease: CITRULLINEMIA, TYPE II, NEONATAL-ONSET
CITRULLINEMIA, TYPE II, NEONATAL-ONSET 		10 0 5 0.25 0 0
CUI: C0158447
Disease: Idiopathic osteoporosis
Idiopathic osteoporosis 		10 0 4 0.19 0 0
CUI: C0268312
Disease: Progressive intrahepatic cholestasis (disorder)
Progressive intrahepatic cholestasis (disorder) 		31 0 7 0.18 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency 		18 0 5 0.18 0 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice 		33 0 7 0.17 0 0
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome 		38 0 7 0.15 0 0
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		38 0 7 0.15 0 0
CUI: C0311361
Disease: Adenomatous goiter
Adenomatous goiter 		23 0 5 0.15 0 0
CUI: C0860204
Disease: Cholestatic liver disease
Cholestatic liver disease 		58 0 9 0.14 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia 		26 0 5 0.14 0 0
CUI: C0265029
Disease: Portal vein obstruction
Portal vein obstruction 		2 0 2 0.13 0 0
CUI: C0342635
Disease: Hungry bone syndrome
Hungry bone syndrome 		2 0 2 0.13 0 0
CUI: C0948825
Disease: Systremma
Systremma 		2 0 2 0.13 0 0
CUI: C0814152
Disease: Viral hepatitis, type G
Viral hepatitis, type G 		11 0 3 0.13 0 0
CUI: C0266242
Disease: Congenital hypoplasia of bile duct
Congenital hypoplasia of bile duct 		3 0 2 0.12 0 0
CUI: C0348454
Disease: Other hypoparathyroidism
Other hypoparathyroidism 		3 0 2 0.12 0 0
CUI: C0587044
Disease: Left ventricular thrombus
Left ventricular thrombus 		3 0 2 0.12 0 0