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 4 6 0.35 1 0.20
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 6 0.35 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 27 6 0.35 1 3.6E-02
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 0.35 0 0
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 7 0.29 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 4 8 0.28 1 0.20
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 6 0.27 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 6 0.25 0 0
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 6 0.24 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 6 0.24 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 15 8 0.21 1 6.2E-02
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 478 7 0.18 1 2.1E-03
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 29 8 0.17 1 3.3E-02
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 9 0.16 0 0
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		2 1 2 0.14 1 0.50
CUI: C0742803
Disease: Conus Medullaris Syndrome
Conus Medullaris Syndrome 		3 0 2 0.13 0 0
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		75 0 10 0.13 0 0
CUI: C1859518
Disease: Beta-Aminoisobutyric Acid, Urinary Excretion of
Beta-Aminoisobutyric Acid, Urinary Excretion of 		4 0 2 0.12 0 0
CUI: C0342751
Disease: Generalized glycogen storage disease of infants
Generalized glycogen storage disease of infants 		51 0 7 0.12 0 0
CUI: C0272238
Disease: Transient hypogammaglobulinemia of infancy
Transient hypogammaglobulinemia of infancy 		5 0 2 0.12 0 0
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 7 0.12 0 0
CUI: C1263988
Disease: Hemolytic disorder
Hemolytic disorder 		15 0 3 0.12 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 2 0.11 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 535 7 0.11 1 1.9E-03
CUI: C2242816
Disease: Chronic secretory otitis media
Chronic secretory otitis media 		6 0 2 0.11 0 0