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: C0206019
Disease: HIV Encephalopathy
HIV Encephalopathy
45 0 3 4.6E-02 0 0
Familial hypercholesterolemia - homozygous
23 0 2 4.5E-02 0 0
CUI: C1142339
Disease: Intestinal adenoma
Intestinal adenoma
23 0 2 4.5E-02 0 0
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation
23 0 2 4.5E-02 0 0
CUI: C0020623
Disease: Hypolipoproteinemias
Hypolipoproteinemias
1 0 1 4.3E-02 0 0
CUI: C0026961
Disease: Mydriasis
Mydriasis
25 0 2 4.3E-02 0 0
CUI: C0035326
Disease: Retinal vascular occlusion
Retinal vascular occlusion
1 0 1 4.3E-02 0 0
CUI: C0236656
Disease: Dementia associated with alcoholism
Dementia associated with alcoholism
1 0 1 4.3E-02 0 0
CUI: C0276044
Disease: Contagious bovine pleuropneumonia
Contagious bovine pleuropneumonia
1 0 1 4.3E-02 0 0
CUI: C0311343
Disease: Membranous conjunctivitis
Membranous conjunctivitis
1 0 1 4.3E-02 0 0
CUI: C0339495
Disease: Cilioretinal artery occlusion
Cilioretinal artery occlusion
1 0 1 4.3E-02 0 0
Cytosolic acetoacetyl-CoA thiolase deficiency
1 0 1 4.3E-02 0 0
Tetralogy of Fallot with pulmonary atresia
1 0 1 4.3E-02 0 0
Imbalance of constituents of food intake
1 0 1 4.3E-02 0 0
CUI: C0349086
Disease: Delirium co-occurrent with dementia
Delirium co-occurrent with dementia
1 0 1 4.3E-02 0 0
CUI: C0393664
Disease: Multiple Sclerosis, Acute Relapsing
Multiple Sclerosis, Acute Relapsing
1 0 1 4.3E-02 0 0
Apolipoproteins E measurement (procedure)
1 0 1 4.3E-02 0 0
CUI: C0574014
Disease: Axillary vein thrombosis
Axillary vein thrombosis
1 0 1 4.3E-02 0 0
CUI: C0581386
Disease: Chronic anxiety
Chronic anxiety
1 0 1 4.3E-02 0 0
CUI: C0860628
Disease: Loss of memory ability
Loss of memory ability
1 0 1 4.3E-02 0 0
CUI: C1274355
Disease: Streptococcal infection of skin
Streptococcal infection of skin
1 0 1 4.3E-02 0 0
CUI: C1388177
Disease: Arteriosclerosis of aorta
Arteriosclerosis of aorta
1 0 1 4.3E-02 0 0
CUI: C1389273
Disease: Lesions in the basal ganglia
Lesions in the basal ganglia
1 0 1 4.3E-02 0 0
CUI: C1720772
Disease: Hypoprebetalipoproteinemia
Hypoprebetalipoproteinemia
1 0 1 4.3E-02 0 0
CUI: C1835362
Disease: Lp(A) Deficiency, Congenital
Lp(A) Deficiency, Congenital
1 0 1 4.3E-02 0 0