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: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic
13 0 13 0.81 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
31 0 13 0.38 0 0
CUI: C0520572
Disease: Enzymopathy
Enzymopathy
17 0 5 0.18 0 0
Anemia, Hemolytic, Congenital Nonspherocytic
5 0 3 0.17 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital
27 0 6 0.16 0 0
CUI: C0002891
Disease: Anemia, Neonatal
Anemia, Neonatal
6 0 3 0.16 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises
7 0 3 0.15 0 0
CUI: C1263988
Disease: Hemolytic disorder
Hemolytic disorder
15 0 4 0.15 0 0
Chronic non-spherocytic hemolytic anemia
2 0 2 0.12 0 0
Deficiency of glucose-6-phosphate isomerase
2 0 2 0.12 0 0
CUI: C0242183
Disease: Jaundice, Hemolytic
Jaundice, Hemolytic
3 0 2 0.12 0 0
Glutamate-cysteine ligase deficiency
3 0 2 0.12 0 0
CUI: C3554330
Disease: NEPHROTIC SYNDROME, TYPE 7
NEPHROTIC SYNDROME, TYPE 7
3 11 2 0.12 1 9.1E-02
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 7
3 5 2 0.12 1 0.20
CUI: C2242796
Disease: Sickle cell-thalassemia disease
Sickle cell-thalassemia disease
4 0 2 0.11 0 0
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia
15 0 3 0.11 0 0
Anemia, hereditary spherocytic hemolytic
5 0 2 0.11 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis
5 0 2 0.11 0 0
CUI: C1336820
Disease: Treatment-Induced Anemia
Treatment-Induced Anemia
5 0 2 0.11 0 0
MALARIA, SUSCEPTIBILITY TO (finding)
5 0 2 0.11 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility
6 0 2 1.0E-01 0 0
CUI: C0019054
Disease: Hemolysis (disorder)
Hemolysis (disorder)
6 0 2 1.0E-01 0 0
CUI: C0312854
Disease: Extravascular Hemolysis
Extravascular Hemolysis
6 0 2 1.0E-01 0 0
CUI: C0019048
Disease: Hemoglobinuria
Hemoglobinuria
8 0 2 9.1E-02 0 0
Chronic hepatitis C virus genotype 1
8 0 2 9.1E-02 0 0