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: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		0 28 0 0 1 2.2E-03
CUI: C0033707
Disease: Prothrombin time assay
Prothrombin time assay 		0 2 0 0 1 2.3E-03
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 2.2E-03
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0 212 0 0 1 1.6E-03
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 2.2E-03
CUI: C0853879
Disease: Invasive carcinoma of breast
Invasive carcinoma of breast 		0 21 0 0 1 2.2E-03
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0 35 0 0 1 2.2E-03
CUI: C3890352
Disease: P-Selectin Measurement
P-Selectin Measurement 		0 2 0 0 1 2.3E-03
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement 		0 3 0 0 1 2.3E-03
CUI: C4722224
Disease: Vascular Endothelial Growth Factor Receptor 2 Measurement
Vascular Endothelial Growth Factor Receptor 2 Measurement 		0 2 0 0 1 2.3E-03
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum 		1 0 1 1.8E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 1.8E-02 0 0
CUI: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement 		1 0 1 1.8E-02 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord 		1 0 1 1.8E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 1.8E-02 0 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage 		1 0 1 1.8E-02 0 0
CUI: C0270027
Disease: Antepartum hemorrhage affecting fetus or newborn
Antepartum hemorrhage affecting fetus or newborn 		1 0 1 1.8E-02 0 0
CUI: C0272240
Disease: Disorder of complement
Disorder of complement 		1 0 1 1.8E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 1.8E-02 0 0
CUI: C0272327
Disease: Hereditary factor X deficiency disease
Hereditary factor X deficiency disease 		1 0 1 1.8E-02 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 1.8E-02 0 0
CUI: C0272334
Disease: Hereditary factor XII deficiency disease
Hereditary factor XII deficiency disease 		1 0 1 1.8E-02 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 1.8E-02 0 0
CUI: C0272356
Disease: von Willebrand disease, type IID
von Willebrand disease, type IID 		1 0 1 1.8E-02 0 0
CUI: C0333183
Disease: Partial stenosis
Partial stenosis 		1 0 1 1.8E-02 0 0