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: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2
16 0 12 0.57 0 0
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder)
9 4 9 0.53 2 5.0E-02
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
9 3 9 0.53 2 5.1E-02
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2
9 27 9 0.53 11 0.20
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia
23 4 12 0.43 1 2.4E-02
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding)
14 8 9 0.41 2 4.5E-02
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin
17 1 9 0.36 1 2.6E-02
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
33 0 13 0.35 0 0
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection
9 0 6 0.30 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder)
40 29 13 0.30 6 9.8E-02
CUI: C0022610
Disease: Kernicterus
Kernicterus
17 0 7 0.26 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
32 478 9 0.23 2 3.9E-03
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia
53 0 12 0.21 0 0
Generalized glycogen storage disease of infants
51 0 10 0.17 0 0
Xeroderma Pigmentosum, Complementation Group D
70 0 12 0.16 0 0
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection
72 0 12 0.16 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
56 535 9 0.14 2 3.5E-03
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice
59 14 9 0.13 1 2.0E-02
Malignant Female Reproductive System Neoplasm
47 0 7 0.12 0 0
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
48 0 7 0.12 0 0
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised
67 6 9 0.12 1 2.3E-02
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
131 0 15 0.11 0 0
Deficiency of glucose-6-phosphate dehydrogenase
75 0 8 9.5E-02 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis
53 0 6 9.4E-02 0 0