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: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 2 0.14 3 0.11
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 2 0.14 2 7.4E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 2 0.14 3 0.11
CUI: C0740989
Disease: Chronic iron deficiency anaemia
Chronic iron deficiency anaemia 		2 0 1 0.14 0 0
CUI: C0854440
Disease: Fatty acid deficiency
Fatty acid deficiency 		2 0 1 0.14 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 3 1 0.14 1 8.3E-02
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		2 3 1 0.14 1 8.3E-02
CUI: C2936913
Disease: Porphyria, South African type
Porphyria, South African type 		2 0 1 0.14 0 0
CUI: C4551590
Disease: Familial renal hypouricemia
Familial renal hypouricemia 		2 0 1 0.14 0 0
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 35 3 0.13 2 4.7E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 35 3 0.13 2 4.7E-02
CUI: C0347176
Disease: Carcinoma in situ of fallopian tube
Carcinoma in situ of fallopian tube 		3 0 1 0.12 0 0
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		3 1 1 0.12 1 1.0E-01
CUI: C1858664
Disease: HEMOCHROMATOSIS, TYPE 3
HEMOCHROMATOSIS, TYPE 3 		3 0 1 0.12 0 0
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 1 0.12 0 0
CUI: C0202171
Disease: Phosphatidylinositol measurement
Phosphatidylinositol measurement 		4 0 1 0.11 0 0
CUI: C0581874
Disease: Late insomnia
Late insomnia 		4 0 1 0.11 0 0
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		4 3 1 0.11 1 8.3E-02
CUI: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
HEMOCHROMATOSIS, TYPE 4 		4 0 1 0.11 0 0
CUI: C2316832
Disease: Arachidonic acid measurement
Arachidonic acid measurement 		4 4 1 0.11 1 7.7E-02
CUI: C3839044
Disease: Compensated liver disease
Compensated liver disease 		4 0 1 0.11 0 0
CUI: C4552187
Disease: Cardiac iron overload
Cardiac iron overload 		4 0 1 0.11 0 0
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 36 3 0.10 4 9.5E-02
CUI: C0031873
Disease: Pica Disease
Pica Disease 		5 3 1 1.0E-01 1 8.3E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		5 4 1 1.0E-01 1 7.7E-02