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: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia 		0 13 0 0 1 3.6E-02
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		0 3 0 0 1 5.6E-02
CUI: C0033802
Disease: Pseudogout
Pseudogout 		0 5 0 0 1 5.0E-02
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 6.2E-02
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		0 10 0 0 1 4.0E-02
CUI: C0238158
Disease: Secondary hemochromatosis
Secondary hemochromatosis 		0 1 0 0 1 6.2E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 4.8E-02
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 4 0 0 1 5.3E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 2.8E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		0 10 0 0 1 4.0E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0 19 0 0 1 2.9E-02
CUI: C0553730
Disease: Calcium pyrophosphate deposition disease
Calcium pyrophosphate deposition disease 		0 5 0 0 1 5.0E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 2.8E-02
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0 35 0 0 1 2.0E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 1 5.9E-02
CUI: C0869532
Disease: Beta thalassemia minor
Beta thalassemia minor 		0 1 0 0 1 6.2E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 5.9E-02
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 5.6E-02
CUI: C1262289
Disease: Dysmetabolic syndrome
Dysmetabolic syndrome 		0 1 0 0 1 6.2E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 5.9E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 5.6E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0 35 0 0 1 2.0E-02
CUI: C1290073
Disease: Acute mucositis
Acute mucositis 		0 1 0 0 1 6.2E-02
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0 95 0 0 1 9.1E-03
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 1 5.6E-02