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: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 36 12 0.39 13 0.27
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 4 0.17 3 0.12
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 16 4 0.16 5 0.14
CUI: C0428578
Disease: Iron level result
Iron level result 		12 16 4 0.16 5 0.14
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 3 0.15 4 0.13
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 3 0.15 4 0.13
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 3 0.12 4 9.5E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 3 0.12 4 9.5E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 35 4 0.12 2 3.4E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 35 4 0.12 2 3.4E-02
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		3 20 2 0.11 1 2.3E-02
CUI: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
HEMOCHROMATOSIS, TYPE 4 		4 0 2 0.11 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 3 0.10 3 0.12
CUI: C0268060
Disease: Juvenile hemochromatosis
Juvenile hemochromatosis 		18 8 3 9.4E-02 1 3.1E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		7 26 2 9.1E-02 4 8.5E-02
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 2 8.0E-02 0 0
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 2 8.0E-02 3 7.3E-02
CUI: C0268059
Disease: Neonatal hemochromatosis
Neonatal hemochromatosis 		13 0 2 7.1E-02 0 0
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		18 1 2 6.1E-02 1 4.0E-02
CUI: C0007862
Disease: Cervico-Brachial Neuralgia
Cervico-Brachial Neuralgia 		1 0 1 5.9E-02 0 0
CUI: C0085920
Disease: Brachial Neuralgia
Brachial Neuralgia 		1 0 1 5.9E-02 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 5.9E-02 1 4.0E-02
CUI: C0268072
Disease: Hypercupremia
Hypercupremia 		1 0 1 5.9E-02 0 0
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder 		1 0 1 5.9E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 5.9E-02 0 0