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: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia
2 0 2 0.67 0 0
CUI: C0236656
Disease: Dementia associated with alcoholism
Dementia associated with alcoholism
1 0 1 0.33 0 0
CUI: C0342889
Disease: Secondary hypertriglyceridemia
Secondary hypertriglyceridemia
1 0 1 0.33 0 0
Tetralogy of Fallot with pulmonary atresia
1 0 1 0.33 0 0
Imbalance of constituents of food intake
1 0 1 0.33 0 0
CUI: C0349086
Disease: Delirium co-occurrent with dementia
Delirium co-occurrent with dementia
1 0 1 0.33 0 0
CUI: C0393664
Disease: Multiple Sclerosis, Acute Relapsing
Multiple Sclerosis, Acute Relapsing
1 0 1 0.33 0 0
Apolipoproteins E measurement (procedure)
1 0 1 0.33 0 0
CUI: C0581386
Disease: Chronic anxiety
Chronic anxiety
1 0 1 0.33 0 0
CUI: C0860628
Disease: Loss of memory ability
Loss of memory ability
1 0 1 0.33 0 0
CUI: C1096710
Disease: Lactescent serum
Lactescent serum
1 0 1 0.33 0 0
CUI: C1388177
Disease: Arteriosclerosis of aorta
Arteriosclerosis of aorta
1 0 1 0.33 0 0
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
1 0 1 0.33 0 0
Hypothalamic-pituitary-adrenal axis dysfunction
1 0 1 0.33 0 0
CUI: C2921138
Disease: Visuospatial deficit
Visuospatial deficit
1 0 1 0.33 0 0
Familial hyperchylomicronemia syndrome
5 0 2 0.33 0 0
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
1 0 1 0.33 0 0
CUI: C3810349
Disease: ALZHEIMER DISEASE 19
ALZHEIMER DISEASE 19
1 0 1 0.33 0 0
CUI: C3825107
Disease: Hypertension in old age
Hypertension in old age
1 0 1 0.33 0 0
CUI: C3825452
Disease: Depression in old age
Depression in old age
1 0 1 0.33 0 0
CUI: C4015869
Disease: APOE2-DUNEDIN PHENOTYPE
APOE2-DUNEDIN PHENOTYPE
1 0 1 0.33 0 0
CUI: C4015877
Disease: APOE3(-)-FREIBURG PHENOTYPE
APOE3(-)-FREIBURG PHENOTYPE
1 0 1 0.33 0 0
CUI: C4015878
Disease: APOE4 VARIANT PHENOTYPE
APOE4 VARIANT PHENOTYPE
1 0 1 0.33 0 0
CUI: C4015880
Disease: APOE2 VARIANT PHENOTYPE
APOE2 VARIANT PHENOTYPE
1 0 1 0.33 0 0
CUI: C4015881
Disease: APOE4(+) PHENOTYPE
APOE4(+) PHENOTYPE
1 0 1 0.33 0 0