Source: INFERRED ×
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: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 12 0.39 13 0.27
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		20 35 5 0.12 4 6.0E-02
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		20 35 5 0.12 4 6.0E-02
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 16 4 0.12 3 6.1E-02
CUI: C0428578
Disease: Iron level result
Iron level result 		12 16 4 0.12 3 6.1E-02
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis 		4 16 3 0.11 2 4.0E-02
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 3 0.10 4 9.5E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 3 0.10 4 9.5E-02
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		3 12 2 7.4E-02 2 4.3E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		7 26 2 6.5E-02 3 5.1E-02
CUI: C0151900
Disease: Serum iron raised
Serum iron raised 		10 0 2 5.9E-02 0 0
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 2 5.9E-02 3 5.6E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 2 5.9E-02 2 3.8E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 2 5.9E-02 3 5.6E-02
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		11 0 2 5.7E-02 0 0
CUI: C0221281
Disease: Poikilocytosis
Poikilocytosis 		14 0 2 5.3E-02 0 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement 		15 0 2 5.1E-02 0 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis 		16 0 2 5.0E-02 0 0
CUI: C4551761
Disease: Excessive daytime sleepiness
Excessive daytime sleepiness 		19 0 2 4.7E-02 0 0
CUI: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		23 0 2 4.3E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		1 0 1 3.8E-02 0 0
CUI: C0236663
Disease: Alcohol withdrawal syndrome
Alcohol withdrawal syndrome 		1 0 1 3.8E-02 0 0
CUI: C1834304
Disease: AMYOTROPHY, HEREDITARY NEURALGIC
AMYOTROPHY, HEREDITARY NEURALGIC 		1 0 1 3.8E-02 0 0
CUI: C1837229
Disease: Muscular Dystrophy, Congenital, Type 1D
Muscular Dystrophy, Congenital, Type 1D 		1 0 1 3.8E-02 0 0
CUI: C1857663
Disease: Yunis Varon syndrome
Yunis Varon syndrome 		1 0 1 3.8E-02 0 0