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: C0162701
Disease: Polysomnography
Polysomnography 		0 249 0 0 1 3.5E-03
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0 79 0 0 1 8.8E-03
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm 		0 2 0 0 1 2.8E-02
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0 116 0 0 1 6.7E-03
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease 		0 40 0 0 1 1.4E-02
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0 427 0 0 1 2.2E-03
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
SPHEROCYTOSIS, TYPE 1 (disorder) 		0 16 0 0 1 2.0E-02
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD 		0 40 0 0 1 1.4E-02
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement 		0 3 0 0 1 2.7E-02
CUI: C4290140
Disease: recurrent myocardial infarction
recurrent myocardial infarction 		0 6 0 0 2 5.1E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0 4389 0 0 1 2.3E-04
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
Large-artery atherosclerosis (embolus/thrombosis) 		0 35 0 0 1 1.4E-02
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement 		0 6 0 0 1 2.5E-02
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		973 0 1 1.0E-03 0 0
CUI: C0494165
Disease: Secondary malignant neoplasm of liver
Secondary malignant neoplasm of liver 		951 0 1 1.0E-03 0 0
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions 		929 0 1 1.0E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 1 1.1E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.1E-03 0 0
CUI: C0021400
Disease: Influenza
Influenza 		858 0 1 1.1E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 1 1.1E-03 0 0
CUI: C0029453
Disease: Osteopenia
Osteopenia 		845 0 1 1.2E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 0 1 1.2E-03 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 1 1.2E-03 0 0
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		757 0 1 1.3E-03 0 0
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma 		724 0 1 1.3E-03 0 0