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: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 0 6 0.50 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 6 0.50 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 6 0.50 0 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 6 0.35 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 6 0.35 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 6 0.32 0 0
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 6 0.30 0 0
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 6 0.30 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 6 0.30 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 0 6 0.23 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 6 0.17 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 6 0.17 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 6 0.14 0 0
CUI: C0699889
Disease: Malignant Female Reproductive System Neoplasm
Malignant Female Reproductive System Neoplasm 		47 0 6 0.12 0 0
CUI: C0268309
Disease: Inherited disorder of bilirubin metabolism
Inherited disorder of bilirubin metabolism 		1 0 1 0.11 0 0
CUI: C0338329
Disease: recurrent childhood brain stem glioma
recurrent childhood brain stem glioma 		1 0 1 0.11 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 6 0.11 0 0
CUI: C0431603
Disease: Ectopic liver
Ectopic liver 		1 0 1 0.11 0 0
CUI: C0473118
Disease: Physiological hyperbilirubinemia (disorder)
Physiological hyperbilirubinemia (disorder) 		1 0 1 0.11 0 0
CUI: C1531394
Disease: Perinatal jaundice
Perinatal jaundice 		1 0 1 0.11 0 0
CUI: C2350171
Disease: Bilateral Nasal Obstruction
Bilateral Nasal Obstruction 		1 0 1 0.11 0 0
CUI: C3502107
Disease: Breastfeeding Jaundice
Breastfeeding Jaundice 		1 0 1 0.11 0 0
CUI: C3888554
Disease: UGT1A1 gene polymorphism
UGT1A1 gene polymorphism 		1 0 1 0.11 0 0
CUI: C4024698
Disease: Diaminoaciduria
Diaminoaciduria 		1 0 1 0.11 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 6 0.11 0 0