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 9 0.53 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 9 0.53 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 9 0.53 0 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 9 0.41 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 9 0.38 0 0
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 38 9 0.36 1 2.6E-02
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 0.30 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 0 9 0.29 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 6 0.24 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 9 0.23 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 9 0.22 0 0
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 6 0.21 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 9 0.19 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 10 0.17 0 0
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 9 0.15 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 9 0.14 0 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 14 9 0.13 1 7.1E-02
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		67 6 9 0.12 1 0.17
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 9 0.12 0 0
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		72 0 9 0.11 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas 		13 0 3 0.11 0 0
CUI: C0699889
Disease: Malignant Female Reproductive System Neoplasm
Malignant Female Reproductive System Neoplasm 		47 0 6 0.10 0 0
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		48 0 6 0.10 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 6 9.4E-02 0 0
CUI: C4255088
Disease: Isolated polycystic liver disease
Isolated polycystic liver disease 		7 0 2 9.1E-02 0 0