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: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder 		0 2 0 0 1 4.0E-02
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		0 10 0 0 1 3.0E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 3.4E-02
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		0 2 0 0 1 4.0E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 4 0 0 1 3.7E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 2.3E-02
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 4.2E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		0 10 0 0 1 3.0E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0 19 0 0 1 2.4E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 2.3E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0 35 0 0 1 1.7E-02
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 4.2E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 3.8E-02
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		0 1 0 0 1 4.2E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 4.0E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0 35 0 0 1 1.7E-02
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 1 3.8E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0 26 0 0 1 2.0E-02
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		0 1 0 0 1 4.2E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		0 1 0 0 1 4.2E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		0 2 0 0 1 4.0E-02
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		0 3 0 0 1 3.8E-02
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		0 1 0 0 1 4.2E-02
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 4.0E-02
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		0 2 0 0 1 4.0E-02