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: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 0 16 0.29 0 0
CUI: C0019025
Disease: Hemoglobin F Disease
Hemoglobin F Disease 		27 0 18 0.29 0 0
CUI: C0002875
Disease: Cooley's anemia
Cooley's anemia 		144 0 41 0.26 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 0 14 0.23 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 15 0.21 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 12 0.21 0 0
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 12 0.21 0 0
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		198 103 43 0.21 2 1.8E-02
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 37 23 0.20 3 7.1E-02
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 0 9 0.17 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 9 0.17 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 9 0.17 0 0
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia 		92 0 21 0.17 0 0
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia 		156 44 30 0.17 1 2.0E-02
CUI: C0039730
Disease: Thalassemia
Thalassemia 		136 18 27 0.17 1 4.0E-02
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 13 0.16 0 0
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait 		34 0 12 0.16 0 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 9 0.16 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 9 0.15 0 0
CUI: C0019045
Disease: Hemoglobinopathies
Hemoglobinopathies 		80 43 17 0.15 1 2.0E-02
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 13 13 0.14 1 5.0E-02
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		37 0 11 0.14 0 0
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease 		29 0 10 0.14 0 0
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		72 0 15 0.14 0 0
CUI: C0085576
Disease: Iron-Refractory Iron Deficiency Anemia
Iron-Refractory Iron Deficiency Anemia 		51 0 12 0.13 0 0