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: C0337439
Disease: Iron measurement
Iron measurement 		12 16 1 5.6E-02 1 4.5E-02
CUI: C0428578
Disease: Iron level result
Iron level result 		12 16 1 5.6E-02 1 4.5E-02
CUI: C0221281
Disease: Poikilocytosis
Poikilocytosis 		14 0 1 5.0E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 0 1 4.8E-02 0 0
CUI: C1846449
Disease: Irregular epiphyses
Irregular epiphyses 		15 0 1 4.8E-02 0 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement 		15 0 1 4.8E-02 0 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis 		16 0 1 4.5E-02 0 0
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 1 4.3E-02 1 3.2E-02
CUI: C0032209
Disease: Platybasia
Platybasia 		18 0 1 4.2E-02 0 0
CUI: C0268060
Disease: Juvenile hemochromatosis
Juvenile hemochromatosis 		18 0 1 4.2E-02 0 0
CUI: C0149955
Disease: Annular pancreas
Annular pancreas 		19 0 1 4.0E-02 0 0
CUI: C4316788
Disease: Abnormality of the intestine
Abnormality of the intestine 		19 0 1 4.0E-02 0 0
CUI: C0265290
Disease: Metaphyseal chondrodysplasia
Metaphyseal chondrodysplasia 		20 0 1 3.8E-02 0 0
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia 		20 0 1 3.8E-02 0 0
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		23 0 1 3.4E-02 0 0
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		25 0 1 3.2E-02 0 0
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		26 36 1 3.1E-02 1 2.4E-02
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia 		26 0 1 3.1E-02 0 0
CUI: C0549306
Disease: Mesomelia
Mesomelia 		27 0 1 3.0E-02 0 0
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder 		29 0 1 2.9E-02 0 0
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance 		29 0 1 2.9E-02 0 0
CUI: C0038506
Disease: Stuttering
Stuttering 		34 0 1 2.5E-02 0 0
CUI: C1838662
Disease: Metaphyseal irregularity
Metaphyseal irregularity 		34 0 1 2.5E-02 0 0
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		37 0 1 2.3E-02 0 0
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		83 62 2 2.3E-02 2 3.0E-02