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: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary 		23 0 12 0.52 0 0
CUI: C1849478
Disease: Increased red cell osmotic fragility
Increased red cell osmotic fragility 		9 0 6 0.40 0 0
CUI: C0221409
Disease: Anemia, hereditary spherocytic hemolytic
Anemia, hereditary spherocytic hemolytic 		5 0 4 0.31 0 0
CUI: C0553720
Disease: Spherocytosis
Spherocytosis 		5 0 4 0.31 0 0
CUI: C4025184
Disease: Spontaneous hemolytic crises
Spontaneous hemolytic crises 		7 0 4 0.27 0 0
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result 		13 0 5 0.25 0 0
CUI: C1846242
Disease: Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis 		4 0 3 0.23 0 0
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia 		15 0 5 0.23 0 0
CUI: C4531297
Disease: Increased mean corpuscular hemoglobin concentration
Increased mean corpuscular hemoglobin concentration 		13 0 4 0.19 0 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		40 0 8 0.18 0 0
CUI: C0018952
Disease: Extramedullary Hematopoiesis Function
Extramedullary Hematopoiesis Function 		16 0 4 0.17 0 0
CUI: C0423791
Disease: Maculopapular Lesion
Maculopapular Lesion 		16 0 4 0.17 0 0
CUI: C0085593
Disease: Chills
Chills 		34 0 6 0.15 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital 		27 0 5 0.15 0 0
CUI: C0002891
Disease: Anemia, Neonatal
Anemia, Neonatal 		6 0 2 0.12 0 0
CUI: C0239937
Disease: Microscopic hematuria
Microscopic hematuria 		15 0 3 0.12 0 0
CUI: C0855790
Disease: Decreased mean corpuscular volume
Decreased mean corpuscular volume 		6 0 2 0.12 0 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement 		15 0 3 0.12 0 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis 		16 0 3 0.12 0 0
CUI: C2674219
Disease: SPHEROCYTOSIS, HEREDITARY, 2
SPHEROCYTOSIS, HEREDITARY, 2 		8 0 2 0.11 0 0
CUI: C1862322
Disease: Ovalocytosis, Malaysian-Melanesian-Filipino Type
Ovalocytosis, Malaysian-Melanesian-Filipino Type 		9 0 2 0.11 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 4 9.8E-02 0 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic 		13 0 2 8.7E-02 0 0
CUI: C0009769
Disease: Conjunctivitis, Giant Papillary
Conjunctivitis, Giant Papillary 		1 0 1 8.3E-02 0 0
CUI: C0266742
Disease: Asymmetrical conjoined twins
Asymmetrical conjoined twins 		1 0 1 8.3E-02 0 0