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: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 92 9 0.12 10 6.7E-02
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		23 33 4 7.8E-02 1 1.0E-02
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity 		26 63 4 7.4E-02 2 1.6E-02
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE 		26 63 4 7.4E-02 2 1.6E-02
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		17 44 3 6.5E-02 1 9.0E-03
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		51 205 5 6.4E-02 1 3.7E-03
CUI: C4022971
Disease: Hyposerinemia
Hyposerinemia 		3 0 2 6.1E-02 0 0
CUI: C4551478
Disease: NEU-LAXOVA SYNDROME 1
NEU-LAXOVA SYNDROME 1 		3 0 2 6.1E-02 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement 		75 422 6 5.9E-02 1 2.0E-03
CUI: C0302274
Disease: Glutamine measurement
Glutamine measurement 		5 5 2 5.7E-02 1 1.4E-02
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		89 0 6 5.2E-02 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		89 0 6 5.2E-02 0 0
CUI: C0523888
Disease: Serine measurement
Serine measurement 		9 18 2 5.1E-02 1 1.2E-02
CUI: C2697764
Disease: Interleukin 16 Measurement
Interleukin 16 Measurement 		9 0 2 5.1E-02 0 0
CUI: C0883409
Disease: Cardiac troponin I measurement
Cardiac troponin I measurement 		11 0 2 4.9E-02 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		55 143 4 4.8E-02 3 1.4E-02
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder) 		14 0 2 4.5E-02 0 0
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement 		14 32 2 4.5E-02 2 2.0E-02
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement 		16 0 2 4.3E-02 0 0
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		20 0 2 4.0E-02 0 0
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary 		54 0 3 3.6E-02 0 0
CUI: C0006114
Disease: Cerebral Edema
Cerebral Edema 		26 0 2 3.6E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 3.1E-02 0 0
CUI: C0406821
Disease: Rhabdomyomatous mesenchymal hamartoma
Rhabdomyomatous mesenchymal hamartoma 		1 0 1 3.1E-02 0 0
CUI: C0580190
Disease: 3-Phosphoglycerate dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency 		1 0 1 3.1E-02 0 0