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: C0005283
Disease: beta Thalassemia
beta Thalassemia 		198 103 90 0.36 14 0.13
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 41 0.26 0 0
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia 		156 44 59 0.24 8 0.15
CUI: C0039730
Disease: Thalassemia
Thalassemia 		136 18 47 0.20 3 8.8E-02
CUI: C0019025
Disease: Hemoglobin F Disease
Hemoglobin F Disease 		27 0 22 0.15 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 37 27 0.13 4 7.7E-02
CUI: C0019045
Disease: Hemoglobinopathies
Hemoglobinopathies 		80 43 26 0.13 2 3.3E-02
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		434 138 66 0.13 12 8.3E-02
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		72 4 24 0.12 2 9.5E-02
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		131 27 30 0.12 1 2.2E-02
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia 		92 16 25 0.12 2 6.1E-02
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 1 16 0.11 1 5.3E-02
CUI: C0037054
Disease: Sickle Cell Trait
Sickle Cell Trait 		75 16 21 0.11 3 9.4E-02
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		75 20 21 0.11 2 5.4E-02
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 13 18 0.10 2 6.7E-02
CUI: C0282193
Disease: Iron Overload
Iron Overload 		241 53 35 1.0E-01 3 4.3E-02
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		154 31 27 1.0E-01 3 6.4E-02
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 16 9.9E-02 0 0
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		37 12 16 9.7E-02 3 0.11
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		230 93 32 9.4E-02 5 4.7E-02
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 0 14 9.2E-02 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 29 15 8.9E-02 1 2.1E-02
CUI: C0238644
Disease: Anemia, severe
Anemia, severe 		65 0 17 8.9E-02 0 0
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 13 8.8E-02 0 0
CUI: C0376154
Disease: Skin callus
Skin callus 		154 0 24 8.8E-02 0 0