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: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 13 11 8.6E-02 1 2.0E-02
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 0 8 8.3E-02 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 9 8.2E-02 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		154 31 18 8.1E-02 1 1.5E-02
CUI: C0238159
Disease: Hemoglobin E disease
Hemoglobin E disease 		8 0 7 8.0E-02 0 0
CUI: C0271986
Disease: delta beta^0^ Thalassemia
delta beta^0^ Thalassemia 		10 0 7 7.9E-02 0 0
CUI: C0271985
Disease: Delta-Beta Thalassemia
Delta-Beta Thalassemia 		12 0 7 7.7E-02 0 0
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		83 21 12 7.6E-02 1 1.8E-02
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		434 138 36 7.4E-02 16 0.10
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 7 7.3E-02 0 0
CUI: C2747816
Disease: Complicated malaria
Complicated malaria 		166 0 17 7.2E-02 0 0
CUI: C0018939
Disease: Hematological Disease
Hematological Disease 		255 16 23 7.2E-02 1 1.9E-02
CUI: C0858321
Disease: Plasmodium vivax infection
Plasmodium vivax infection 		21 0 7 7.0E-02 0 0
CUI: C4543807
Disease: Clinical malaria
Clinical malaria 		37 0 8 7.0E-02 0 0
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		8 2 6 6.8E-02 1 2.6E-02
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 8 6.8E-02 0 0
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 0 6 6.7E-02 0 0
CUI: C0349705
Disease: Abnormal hemoglobin finding
Abnormal hemoglobin finding 		9 0 6 6.7E-02 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 6 6.7E-02 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 6 6.7E-02 0 0
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 6.7E-02 0 0
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		25 0 7 6.7E-02 0 0
CUI: C1845055
Disease: ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED 		42 32 8 6.7E-02 1 1.5E-02
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 6 6.4E-02 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		131 0 13 6.4E-02 0 0