Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE
2 0 2 1.00 0 0
APOLIPOPROTEIN C-II (PARIS) PHENOTYPE
2 0 2 1.00 0 0
APOLIPOPROTEIN C-II (BARI) PHENOTYPE
2 0 2 1.00 0 0
APOLIPOPROTEIN C-II VARIANT PHENOTYPE
2 0 2 1.00 0 0
CUI: C4017137
Disease: APOLIPOPROTEIN C-II (SAN FRANCISCO)
APOLIPOPROTEIN C-II (SAN FRANCISCO)
2 0 2 1.00 0 0
APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE
2 0 2 1.00 0 0
Apolipoprotein C-II Deficiency (disorder)
3 5 2 0.67 1 0.20
CUI: C1274228
Disease: Chylomicronemia syndrome
Chylomicronemia syndrome
2 0 1 0.33 0 0
Familial apolipoprotein C-II deficiency
3 0 1 0.25 0 0
Deficiency of triacylglycerol lipase
3 0 1 0.25 0 0
CUI: C0221252
Disease: Eruptive xanthoma
Eruptive xanthoma
4 0 1 0.20 0 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis
4 0 1 0.20 0 0
Granulocyte Colony Stimulating Factor Measurement
4 0 1 0.20 0 0
Familial hyperchylomicronemia syndrome
5 0 1 0.17 0 0
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia
12 0 1 7.7E-02 0 0
CUI: C4551632
Disease: Recurrent pancreatitis
Recurrent pancreatitis
14 0 1 6.7E-02 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias
20 0 1 4.8E-02 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis
20 0 1 4.8E-02 0 0
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias
20 0 1 4.8E-02 0 0
CUI: C0406537
Disease: Morbilliform Drug Reaction
Morbilliform Drug Reaction
24 0 1 4.0E-02 0 0
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
27 0 1 3.6E-02 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
28 0 1 3.4E-02 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma
29 0 1 3.3E-02 0 0
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I
36 0 1 2.7E-02 0 0
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
39 0 1 2.5E-02 0 0