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: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 9 0.16 0 0
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 8 13 0.14 1 5.0E-02
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia 		24 13 9 0.13 1 4.0E-02
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 8 0.13 0 0
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary 		23 0 8 0.12 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 9 0.12 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		131 0 19 0.12 0 0
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		75 0 13 0.11 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital 		27 0 8 0.11 0 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		40 0 9 0.11 0 0
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 0 6 0.11 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 6 0.11 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 6 0.11 0 0
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 0.11 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 0 7 0.10 0 0
CUI: C0002875
Disease: Cooley's anemia
Cooley's anemia 		144 19 18 0.10 2 6.7E-02
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 6 9.8E-02 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		154 31 18 9.5E-02 4 1.0E-01
CUI: C0018952
Disease: Extramedullary Hematopoiesis Function
Extramedullary Hematopoiesis Function 		16 0 6 9.5E-02 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 6 9.5E-02 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 5 9.4E-02 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 5 9.4E-02 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 29 8 9.4E-02 1 2.4E-02
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 6 9.4E-02 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 6 9.4E-02 0 0