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: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice 		33 0 5 9.1E-02 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 5 9.1E-02 0 0
CUI: C1862322
Disease: Ovalocytosis, Malaysian-Melanesian-Filipino Type
Ovalocytosis, Malaysian-Melanesian-Filipino Type 		9 0 3 9.1E-02 0 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 0 7 8.9E-02 0 0
CUI: C0085577
Disease: Normocytic anemia
Normocytic anemia 		12 0 3 8.3E-02 0 0
CUI: C4531297
Disease: Increased mean corpuscular hemoglobin concentration
Increased mean corpuscular hemoglobin concentration 		13 0 3 8.1E-02 0 0
CUI: C0221281
Disease: Poikilocytosis
Poikilocytosis 		14 0 3 7.9E-02 0 0
CUI: C1263988
Disease: Hemolytic disorder
Hemolytic disorder 		15 0 3 7.7E-02 0 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement 		15 0 3 7.7E-02 0 0
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease 		29 0 4 7.7E-02 0 0
CUI: C0018952
Disease: Extramedullary Hematopoiesis Function
Extramedullary Hematopoiesis Function 		16 0 3 7.5E-02 0 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis 		16 0 3 7.5E-02 0 0
CUI: C0423791
Disease: Maculopapular Lesion
Maculopapular Lesion 		16 0 3 7.5E-02 0 0
CUI: C0024537
Disease: Malaria, Vivax
Malaria, Vivax 		60 0 6 7.4E-02 0 0
CUI: C0031049
Disease: Pericarditis, Tuberculous
Pericarditis, Tuberculous 		2 0 2 7.4E-02 0 0
CUI: C0340969
Disease: Uridine monophosphate hydrolase deficiency
Uridine monophosphate hydrolase deficiency 		2 0 2 7.4E-02 0 0
CUI: C0398561
Disease: Glucose phosphate isomerase deficiency
Glucose phosphate isomerase deficiency 		2 0 2 7.4E-02 0 0
CUI: C0398563
Disease: Deficiency of hexokinase (disorder)
Deficiency of hexokinase (disorder) 		2 0 2 7.4E-02 0 0
CUI: C0472790
Disease: Chronic non-spherocytic hemolytic anemia
Chronic non-spherocytic hemolytic anemia 		2 0 2 7.4E-02 0 0
CUI: C1291611
Disease: Deficiency of glucose-6-phosphate isomerase
Deficiency of glucose-6-phosphate isomerase 		2 0 2 7.4E-02 0 0
CUI: C4693796
Disease: RH-NULL, AMORPH TYPE
RH-NULL, AMORPH TYPE 		2 0 2 7.4E-02 0 0
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 0 3 7.1E-02 0 0
CUI: C0158962
Disease: Hemolytic disease of fetus OR newborn due to RhD isoimmunization
Hemolytic disease of fetus OR newborn due to RhD isoimmunization 		3 0 2 7.1E-02 0 0
CUI: C0272052
Disease: Rh Deficiency Syndrome
Rh Deficiency Syndrome 		3 0 2 7.1E-02 0 0
CUI: C0272105
Disease: Anemia due to infection
Anemia due to infection 		3 0 2 7.1E-02 0 0