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: C4020827
Disease: Neonatal hemolytic anemia
Neonatal hemolytic anemia 		2 0 2 0.40 0 0
CUI: C3841459
Disease: Hb H disease
Hb H disease 		10 0 3 0.25 0 0
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		6 0 2 0.22 0 0
CUI: C0042875
Disease: Vitamin E Deficiency
Vitamin E Deficiency 		6 0 2 0.22 0 0
CUI: C0553699
Disease: Heinz body observation
Heinz body observation 		6 0 2 0.22 0 0
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement 		6 0 2 0.22 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 0.20 0 0
CUI: C0154089
Disease: Carcinoma in situ of penis
Carcinoma in situ of penis 		1 0 1 0.20 0 0
CUI: C0221019
Disease: Sickle cell-beta-thalassemia
Sickle cell-beta-thalassemia 		7 0 2 0.20 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 0.20 0 0
CUI: C0272080
Disease: Hemoglobin D disease
Hemoglobin D disease 		1 0 1 0.20 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 0.20 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 0.20 0 0
CUI: C0429908
Disease: Susceptibility to tuberculosis
Susceptibility to tuberculosis 		1 1 1 0.20 1 4.3E-02
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 0.20 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 0.20 0 0
CUI: C1264000
Disease: Sickle cell-Hemoglobin O Arab disease
Sickle cell-Hemoglobin O Arab disease 		1 0 1 0.20 0 0
CUI: C1332632
Disease: Breast Liposarcoma
Breast Liposarcoma 		1 0 1 0.20 0 0
CUI: C1832168
Disease: BLOOD GROUP--FROESE
BLOOD GROUP--FROESE 		1 2 1 0.20 1 4.2E-02
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		1 14 1 0.20 12 0.48
CUI: C1862190
Disease: BLOOD GROUP--WRIGHT ANTIGEN
BLOOD GROUP--WRIGHT ANTIGEN 		1 2 1 0.20 1 4.2E-02
CUI: C1862191
Disease: BLOOD GROUP--WALDNER TYPE
BLOOD GROUP--WALDNER TYPE 		1 2 1 0.20 1 4.2E-02
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 0.20 0 0
CUI: C1969039
Disease: Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology
Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology 		1 0 1 0.20 0 0
CUI: C1970441
Disease: CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7
CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7 		1 1 1 0.20 1 4.3E-02