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: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias 		3 0 2 0.33 0 0
CUI: C2825560
Disease: S-Beta Thalassemia
S-Beta Thalassemia 		3 0 2 0.33 0 0
CUI: C0271987
Disease: ^A^gamma delta beta^0^ thalassemia
^A^gamma delta beta^0^ thalassemia 		4 0 2 0.29 0 0
CUI: C0472777
Disease: Hemoglobin E/beta thalassemia disease
Hemoglobin E/beta thalassemia disease 		4 0 2 0.29 0 0
CUI: C4023136
Disease: Reduced alpha/beta synthesis ratio
Reduced alpha/beta synthesis ratio 		4 0 2 0.29 0 0
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		10 2 3 0.25 1 0.50
CUI: C3841459
Disease: Hb H disease
Hb H disease 		10 0 3 0.25 0 0
CUI: C4274391
Disease: Dominant beta-thalassemia
Dominant beta-thalassemia 		5 0 2 0.25 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: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 0 4 0.21 0 0
CUI: C0019034
Disease: Hemoglobin SC Disease
Hemoglobin SC Disease 		7 0 2 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: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 0.20 0 0
CUI: C0271990
Disease: delta-Thalassemia
delta-Thalassemia 		7 0 2 0.20 0 0
CUI: C0272080
Disease: Hemoglobin D disease
Hemoglobin D disease 		1 0 1 0.20 0 0
CUI: C0272405
Disease: Functional asplenia
Functional asplenia 		1 0 1 0.20 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		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: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		1 0 1 0.20 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 0.20 1 1.00
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 0.20 1 1.00
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 0.20 1 0.50
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 0.20 1 1.00