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: C2678338
Disease: SPHEROCYTOSIS, TYPE 3 (disorder)
SPHEROCYTOSIS, TYPE 3 (disorder) 		1 0 1 0.14 0 0
CUI: C3149117
Disease: GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE 		1 0 1 0.14 0 0
CUI: C3150730
Disease: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY 		1 0 1 0.14 0 0
CUI: C3553859
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		1 0 1 0.14 0 0
CUI: C4015898
Disease: RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT
RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT 		1 0 1 0.14 0 0
CUI: C4015903
Disease: SWANN BLOOD GROUP ANTIGEN PHENOTYPE
SWANN BLOOD GROUP ANTIGEN PHENOTYPE 		1 0 1 0.14 0 0
CUI: C4015904
Disease: ACANTHOCYTOSIS DUE TO BAND 3 HT
ACANTHOCYTOSIS DUE TO BAND 3 HT 		1 0 1 0.14 0 0
CUI: C4016321
Disease: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, AND NEUROLOGIC DEFICITS, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, AND NEUROLOGIC DEFICITS, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY 		1 0 1 0.14 0 0
CUI: C4016380
Disease: ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL
ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL 		1 0 1 0.14 0 0
CUI: C4017275
Disease: SPHEROCYTOSIS, TYPE 1, AUTOSOMAL RECESSIVE
SPHEROCYTOSIS, TYPE 1, AUTOSOMAL RECESSIVE 		1 0 1 0.14 0 0
CUI: C4022665
Disease: Isothenuria
Isothenuria 		1 0 1 0.14 0 0
CUI: C4304505
Disease: 8p11.2 deletion syndrome
8p11.2 deletion syndrome 		1 0 1 0.14 0 0
CUI: C4551966
Disease: GLUT1 DEFICIENCY SYNDROME 1
GLUT1 DEFICIENCY SYNDROME 1 		1 0 1 0.14 0 0
CUI: C0085593
Disease: Chills
Chills 		34 0 5 0.14 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital 		27 0 4 0.13 0 0
CUI: C0391870
Disease: Abnormality of red blood cells
Abnormality of red blood cells 		2 0 1 0.12 0 0
CUI: C0398561
Disease: Glucose phosphate isomerase deficiency
Glucose phosphate isomerase deficiency 		2 0 1 0.12 0 0
CUI: C0472790
Disease: Chronic non-spherocytic hemolytic anemia
Chronic non-spherocytic hemolytic anemia 		2 0 1 0.12 0 0
CUI: C1096154
Disease: Kinsbourne Syndrome
Kinsbourne Syndrome 		2 0 1 0.12 0 0
CUI: C1291611
Disease: Deficiency of glucose-6-phosphate isomerase
Deficiency of glucose-6-phosphate isomerase 		2 0 1 0.12 0 0
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 0 1 0.12 0 0
CUI: C2675192
Disease: Spherocytosis, Type 5
Spherocytosis, Type 5 		2 0 1 0.12 0 0
CUI: C3278865
Disease: Pigment gallstones
Pigment gallstones 		2 0 1 0.12 0 0
CUI: C4023090
Disease: Impaired neutrophil bactericidal activity
Impaired neutrophil bactericidal activity 		2 0 1 0.12 0 0
CUI: C4023512
Disease: Myoclonic absences
Myoclonic absences 		2 0 1 0.12 0 0