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: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia
0 13 0 0 1 5.9E-02
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders
0 3 0 0 1 0.14
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
0 1 0 0 1 0.20
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder
0 2 0 0 1 0.17
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement
0 10 0 0 1 7.1E-02
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis
0 1 0 0 1 0.20
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
0 8 0 0 1 8.3E-02
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
Cirrhosis, Cryptogenic
0 5 0 0 1 0.11
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda
0 6 0 0 1 1.0E-01
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome
0 4 0 0 1 0.12
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement
0 21 0 0 1 4.0E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement
0 10 0 0 1 7.1E-02
CUI: C0474368
Disease: Labor Pain
Labor Pain
0 1 0 0 1 0.20
Mean corpuscular hemoglobin concentration determination
0 19 0 0 1 4.3E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement
0 21 0 0 1 4.0E-02
Total iron binding capacity function
0 35 0 0 1 2.6E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 0.17
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor
0 1 0 0 1 0.20
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 0.17
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait
0 5 0 0 1 0.11
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder
0 3 0 0 1 0.14
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0 568 0 0 1 1.7E-03
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome
0 1 0 0 1 0.20
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 0.17
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda
0 3 0 0 1 0.14