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: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 4 15 0.37 1 5.6E-02
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 13 0.35 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 12 0.32 0 0
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 4 9 0.27 1 5.6E-02
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 9 0.27 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 27 9 0.27 2 5.0E-02
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 10 0.25 0 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 9 0.24 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 9 0.22 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 29 13 0.22 3 7.3E-02
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 15 0.21 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 2 8 0.21 1 6.2E-02
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 478 10 0.18 4 8.2E-03
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 0 14 0.18 0 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice 		33 2 10 0.18 1 6.2E-02
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		131 27 24 0.17 8 0.24
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 0.17 0 0
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		72 0 14 0.15 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 13 0.14 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 10 0.14 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 535 10 0.13 4 7.3E-03
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		75 0 12 0.12 0 0
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary 		23 0 6 0.12 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 9 0.12 0 0
CUI: C0947622
Disease: Cholecystolithiasis
Cholecystolithiasis 		156 62 19 0.11 1 1.3E-02