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: C1849478
Disease: Increased red cell osmotic fragility
Increased red cell osmotic fragility 		9 0 6 0.20 0 0
CUI: C0520572
Disease: Enzymopathy
Enzymopathy 		17 0 7 0.19 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		5 0 5 0.19 0 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic 		13 0 6 0.18 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired 		16 0 6 0.16 0 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		40 0 9 0.16 0 0
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found 		12 0 5 0.15 0 0
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result 		13 0 5 0.14 0 0
CUI: C4025735
Disease: Nonspherocytic hemolytic anemia
Nonspherocytic hemolytic anemia 		13 0 5 0.14 0 0
CUI: C0002891
Disease: Anemia, Neonatal
Anemia, Neonatal 		6 0 4 0.14 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia 		31 0 7 0.14 0 0
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary 		23 0 6 0.14 0 0
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia 		15 0 5 0.14 0 0
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia 		15 0 5 0.14 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises 		7 0 4 0.13 0 0
CUI: C0235983
Disease: Normochromic anemia
Normochromic anemia 		9 0 4 0.12 0 0
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase 		10 0 4 0.12 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 8 0.11 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		154 0 18 0.11 0 0
CUI: C0085593
Disease: Chills
Chills 		34 0 6 0.11 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 3 0.10 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 3 0.10 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 3 1.0E-01 0 0
CUI: C3666003
Disease: Transfusion dependent anaemia
Transfusion dependent anaemia 		6 0 3 1.0E-01 0 0
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		7 0 3 9.7E-02 0 0