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 0.19 0 0
CUI: C4551984
Disease: Arthrogryposis with renal dysfunction and cholestasis syndrome
Arthrogryposis with renal dysfunction and cholestasis syndrome 		12 0 7 0.18 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 15 10 0.18 1 6.2E-02
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis 		15 0 7 0.17 0 0
CUI: C1859722
Disease: Arthrogryposis, renal dysfunction, and cholestasis 1
Arthrogryposis, renal dysfunction, and cholestasis 1 		16 0 7 0.17 0 0
CUI: C1112213
Disease: Cholestasis in newborn
Cholestasis in newborn 		19 0 7 0.16 0 0
CUI: C0235299
Disease: Right upper quadrant pain
Right upper quadrant pain 		6 0 5 0.15 0 0
CUI: C1867396
Disease: RADIAL-RENAL SYNDROME
RADIAL-RENAL SYNDROME 		6 0 5 0.15 0 0
CUI: C0017927
Disease: Glycogen Storage Disease Type VIII
Glycogen Storage Disease Type VIII 		7 0 5 0.14 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 4 7 0.14 1 0.20
CUI: C0268312
Disease: Progressive intrahepatic cholestasis (disorder)
Progressive intrahepatic cholestasis (disorder) 		31 0 8 0.14 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy 		10 0 5 0.13 0 0
CUI: C1853942
Disease: CITRULLINEMIA, TYPE II, NEONATAL-ONSET
CITRULLINEMIA, TYPE II, NEONATAL-ONSET 		10 0 5 0.13 0 0
CUI: C1827377
Disease: Slow acetylator due to N-acetyltransferase enzyme variant
Slow acetylator due to N-acetyltransferase enzyme variant 		20 0 6 0.13 0 0
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		38 0 8 0.13 0 0
CUI: C0860204
Disease: Cholestatic liver disease
Cholestatic liver disease 		58 0 10 0.12 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 4 0.11 0 0
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		75 20 11 0.11 1 4.8E-02
CUI: C0085280
Disease: Alagille Syndrome
Alagille Syndrome 		38 0 7 0.11 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency 		18 0 5 0.11 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		131 27 16 0.11 1 3.6E-02
CUI: C2880562
Disease: Age-related cortical cataract
Age-related cortical cataract 		9 0 4 0.11 0 0
CUI: C0022346
Disease: Icterus
Icterus 		241 17 26 0.10 1 5.6E-02
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke 		42 0 7 0.10 0 0
CUI: C0311361
Disease: Adenomatous goiter
Adenomatous goiter 		23 0 5 9.8E-02 0 0