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: C0001811
Disease: Aging
Aging 		1 0 1 2.0E-02 0 0
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		1 0 1 2.0E-02 0 0
CUI: C0010201
Disease: Chronic cough
Chronic cough 		1 0 1 2.0E-02 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		1 0 1 2.0E-02 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		1 0 1 2.0E-02 0 0
CUI: C0152169
Disease: Renal Colic
Renal Colic 		1 0 1 2.0E-02 0 0
CUI: C0155196
Disease: Cicatricial ectropion
Cicatricial ectropion 		1 0 1 2.0E-02 0 0
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn 		1 0 1 2.0E-02 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 2 1 2.0E-02 1 4.9E-03
CUI: C0221757
Disease: alpha 1-Antitrypsin Deficiency
alpha 1-Antitrypsin Deficiency 		1 0 1 2.0E-02 0 0
CUI: C0265101
Disease: Carotid artery occlusion
Carotid artery occlusion 		1 0 1 2.0E-02 0 0
CUI: C0272339
Disease: Prekallikrein deficiency
Prekallikrein deficiency 		1 0 1 2.0E-02 0 0
CUI: C0338585
Disease: Dissection of carotid artery
Dissection of carotid artery 		1 0 1 2.0E-02 0 0
CUI: C0342650
Disease: Periarticular calcification
Periarticular calcification 		1 0 1 2.0E-02 0 0
CUI: C0410607
Disease: Intervertebral disk calcification
Intervertebral disk calcification 		1 0 1 2.0E-02 0 0
CUI: C0523509
Disease: Apolipoprotein B Assay
Apolipoprotein B Assay 		1 0 1 2.0E-02 0 0
CUI: C0685661
Disease: Congenital anomaly of ischium
Congenital anomaly of ischium 		1 0 1 2.0E-02 0 0
CUI: C0751815
Disease: Carotid Artery, Internal, Dissection
Carotid Artery, Internal, Dissection 		1 0 1 2.0E-02 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		1 0 1 2.0E-02 0 0
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		1 0 1 2.0E-02 0 0
CUI: C1849508
Disease: EPILEPSY, PYRIDOXINE-DEPENDENT
EPILEPSY, PYRIDOXINE-DEPENDENT 		1 0 1 2.0E-02 0 0
CUI: C1859372
Disease: Calcification of Joints and Arteries
Calcification of Joints and Arteries 		1 0 1 2.0E-02 0 0
CUI: C1859727
Disease: Arterial calcification of infancy
Arterial calcification of infancy 		1 0 1 2.0E-02 0 0
CUI: C1859728
Disease: Coronary Sclerosis, Medial, of Infancy
Coronary Sclerosis, Medial, of Infancy 		1 0 1 2.0E-02 0 0
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		1 0 1 2.0E-02 0 0