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: C0272005
Disease: Hemoglobin Bart's hydrops syndrome
Hemoglobin Bart's hydrops syndrome 		3 0 2 0.22 0 0
CUI: C0272082
Disease: Hemoglobin E trait
Hemoglobin E trait 		3 0 2 0.22 0 0
CUI: C0474543
Disease: Hemoglobin A2 measurement
Hemoglobin A2 measurement 		3 5 2 0.22 1 0.12
CUI: C0521800
Disease: Central cyanosis
Central cyanosis 		3 0 2 0.22 0 0
CUI: C0795917
Disease: Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type
Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type 		3 0 2 0.22 0 0
CUI: C1260396
Disease: Alpha thalassemia intermedia
Alpha thalassemia intermedia 		3 0 2 0.22 0 0
CUI: C2873754
Disease: Severe alpha thalassemia
Severe alpha thalassemia 		3 0 2 0.22 0 0
CUI: C3278365
Disease: HEMOGLOBIN H HYDROPS FETALIS SYNDROME
HEMOGLOBIN H HYDROPS FETALIS SYNDROME 		3 0 2 0.22 0 0
CUI: C3844575
Disease: Hb E beta-thalassemia
Hb E beta-thalassemia 		3 0 2 0.22 0 0
CUI: C1527405
Disease: Erythrocytosis
Erythrocytosis 		9 0 3 0.21 0 0
CUI: C2873756
Disease: Severe beta thalassemia
Severe beta thalassemia 		9 0 3 0.21 0 0
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia 		15 0 4 0.21 0 0
CUI: C0585216
Disease: Alpha-Thalassemia Myelodysplasia Syndrome
Alpha-Thalassemia Myelodysplasia Syndrome 		4 0 2 0.20 0 0
CUI: C0850672
Disease: hereditary anemia
hereditary anemia 		4 0 2 0.20 0 0
CUI: C3841459
Disease: Hb H disease
Hb H disease 		10 0 3 0.20 0 0
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 0 4 0.18 0 0
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		5 0 2 0.18 0 0
CUI: C3539063
Disease: Bart's Hemoglobinopathy
Bart's Hemoglobinopathy 		5 0 2 0.18 0 0
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait 		34 0 6 0.17 0 0
CUI: C4025735
Disease: Nonspherocytic hemolytic anemia
Nonspherocytic hemolytic anemia 		13 0 3 0.17 0 0
CUI: C0271994
Disease: Hereditary persistence of fetal hemoglobin thalassemia
Hereditary persistence of fetal hemoglobin thalassemia 		35 0 6 0.16 0 0
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease 		29 0 5 0.16 0 0
CUI: C0014800
Disease: Erythroid hyperplasia
Erythroid hyperplasia 		22 0 4 0.15 0 0
CUI: C4025630
Disease: Abnormal bone structure
Abnormal bone structure 		7 0 2 0.15 0 0
CUI: C0271933
Disease: Congenital dyserythropoietic anemia, type I
Congenital dyserythropoietic anemia, type I 		8 0 2 0.14 0 0