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: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0 1 0 0 1 3.7E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 3.1E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.7E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 4 0 0 1 3.3E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 2.1E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0 19 0 0 1 2.2E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 2.1E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0 35 0 0 1 1.6E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 3.7E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 1 3.6E-02
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 3.7E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 3.6E-02
CUI: C1095928
Disease: Secondary hyperthyroidism
Secondary hyperthyroidism 		0 1 0 0 1 3.7E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 3.4E-02
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		0 1 0 0 1 3.7E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 3.6E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 3.4E-02
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		0 36 0 0 1 1.6E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0 35 0 0 1 1.6E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		0 25 0 0 1 2.0E-02
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 1 3.4E-02
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.7E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.7E-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 3.6E-02
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		0 3 0 0 1 3.4E-02