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: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 6 1.00 10 1.00
CUI: C0521802
Disease: Congenital atransferrinemia
Congenital atransferrinemia 		3 0 2 0.29 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 3 0.23 2 0.18
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 16 3 0.20 2 8.3E-02
CUI: C0428578
Disease: Iron level result
Iron level result 		12 16 3 0.20 2 8.3E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		7 26 2 0.18 2 5.9E-02
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 3 0.17 2 0.18
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 0.17 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 0.17 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 0.17 1 1.0E-01
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 0.17 1 1.0E-01
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 0.17 1 9.1E-02
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 0.17 1 1.0E-01
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 0.17 0 0
CUI: C3277918
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 0 1 0.17 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 0.17 1 9.1E-02
CUI: C3889615
Disease: TRANSFERRIN VARIANT D1 PHENOTYPE
TRANSFERRIN VARIANT D1 PHENOTYPE 		1 0 1 0.17 0 0
CUI: C3889617
Disease: TRANSFERRIN VARIANT B2 PHENOTYPE
TRANSFERRIN VARIANT B2 PHENOTYPE 		1 0 1 0.17 0 0
CUI: C3889619
Disease: TRANSFERRIN VARIANT Bv PHENOTYPE
TRANSFERRIN VARIANT Bv PHENOTYPE 		1 0 1 0.17 0 0
CUI: C4225610
Disease: TRANSFERRIN VARIANT D(CHI)
TRANSFERRIN VARIANT D(CHI) 		1 0 1 0.17 0 0
CUI: C4703592
Disease: Elevated hepcidin level
Elevated hepcidin level 		1 0 1 0.17 0 0
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 3 0.15 4 0.13
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 0.14 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 1 0.14 1 6.7E-02
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 0.14 0 0