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: C0427480
Disease: Elliptocytosis found
Elliptocytosis found 		12 0 12 0.52 0 0
CUI: C1849478
Disease: Increased red cell osmotic fragility
Increased red cell osmotic fragility 		9 0 7 0.28 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 5 0.22 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 5 0.22 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises 		7 0 5 0.20 0 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		40 0 10 0.19 0 0
CUI: C0085593
Disease: Chills
Chills 		34 0 9 0.19 0 0
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result 		13 0 5 0.16 0 0
CUI: C4531297
Disease: Increased mean corpuscular hemoglobin concentration
Increased mean corpuscular hemoglobin concentration 		13 0 5 0.16 0 0
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia 		15 0 5 0.15 0 0
CUI: C0018952
Disease: Extramedullary Hematopoiesis Function
Extramedullary Hematopoiesis Function 		16 0 5 0.15 0 0
CUI: C0423791
Disease: Maculopapular Lesion
Maculopapular Lesion 		16 0 5 0.15 0 0
CUI: C1862322
Disease: Ovalocytosis, Malaysian-Melanesian-Filipino Type
Ovalocytosis, Malaysian-Melanesian-Filipino Type 		9 0 4 0.14 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital 		27 0 6 0.14 0 0
CUI: C1846242
Disease: Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 		4 0 3 0.12 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 6 0.12 0 0
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 0 8 0.12 0 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement 		15 0 4 0.12 0 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis 		16 0 4 0.11 0 0
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
SPHEROCYTOSIS, TYPE 1 (disorder) 		48 0 7 0.11 0 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic 		13 0 3 9.1E-02 0 0
CUI: C0239937
Disease: Microscopic hematuria
Microscopic hematuria 		15 0 3 8.6E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		41 0 5 8.5E-02 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired 		16 0 3 8.3E-02 0 0
CUI: C0242183
Disease: Jaundice, Hemolytic
Jaundice, Hemolytic 		3 0 2 8.3E-02 0 0