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: C1866810
Disease: ELLIPTOCYTOSIS 3
ELLIPTOCYTOSIS 3
1 9 1 1.00 1 0.11
Anemia, hereditary spherocytic hemolytic
5 0 1 0.20 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis
5 0 1 0.20 0 0
CUI: C1295176
Disease: Leptin measurement
Leptin measurement
5 0 1 0.20 0 0
CUI: C0002891
Disease: Anemia, Neonatal
Anemia, Neonatal
6 0 1 0.17 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises
7 0 1 0.14 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2
8 0 1 0.12 0 0
Increased red cell osmotic fragility
9 0 1 0.11 0 0
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found
12 0 1 8.3E-02 0 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic
13 0 1 7.7E-02 0 0
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result
13 0 1 7.7E-02 0 0
Increased mean corpuscular hemoglobin concentration
13 0 1 7.7E-02 0 0
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia
15 0 1 6.7E-02 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired
16 0 1 6.2E-02 0 0
Extramedullary Hematopoiesis Function
16 0 1 6.2E-02 0 0
CUI: C0423791
Disease: Maculopapular Lesion
Maculopapular Lesion
16 0 1 6.2E-02 0 0
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary
23 0 1 4.3E-02 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital
27 0 1 3.7E-02 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
31 0 1 3.2E-02 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal
33 0 1 3.0E-02 0 0
CUI: C0085593
Disease: Chills
Chills
34 0 1 2.9E-02 0 0
CUI: C0700636
Disease: Focal nodular hyperplasia of liver
Focal nodular hyperplasia of liver
39 0 1 2.6E-02 0 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis
40 0 1 2.5E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy
41 0 1 2.4E-02 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis
47 0 1 2.1E-02 0 0