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: C0428578
Disease: Iron level result
Iron level result 		12 16 12 1.00 16 1.00
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 4 0.22 2 0.12
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 3 0.20 2 8.3E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 3 0.20 2 8.3E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 4 0.16 5 0.14
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 3 0.16 3 8.8E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 3 0.16 3 8.8E-02
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		3 20 2 0.15 1 2.9E-02
CUI: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
HEMOCHROMATOSIS, TYPE 4 		4 0 2 0.14 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 3 0.12 2 0.12
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 36 4 0.12 3 6.1E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		7 26 2 0.12 3 7.7E-02
CUI: C0268060
Disease: Juvenile hemochromatosis
Juvenile hemochromatosis 		18 0 3 0.11 0 0
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 35 3 0.10 1 2.0E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 35 3 0.10 1 2.0E-02
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 2 1.0E-01 0 0
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 2 1.0E-01 2 6.1E-02
CUI: C0268059
Disease: Neonatal hemochromatosis
Neonatal hemochromatosis 		13 0 2 8.7E-02 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 8.3E-02 1 6.2E-02
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 0 1 8.3E-02 0 0
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation 		1 0 1 8.3E-02 0 0
CUI: C0346977
Disease: Secondary malignant neoplasm of spleen
Secondary malignant neoplasm of spleen 		1 0 1 8.3E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 8.3E-02 0 0
CUI: C1313983
Disease: Acute contagious conjunctivitis
Acute contagious conjunctivitis 		1 0 1 8.3E-02 0 0
CUI: C1847024
Disease: ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder) 		1 0 1 8.3E-02 0 0