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: C1291447
Disease: Deficiency of triacylglycerol lipase
Deficiency of triacylglycerol lipase 		3 0 2 0.67 0 0
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		3 0 2 0.67 0 0
CUI: C0221252
Disease: Eruptive xanthoma
Eruptive xanthoma 		4 0 2 0.50 0 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis 		4 0 2 0.50 0 0
CUI: C0342889
Disease: Secondary hypertriglyceridemia
Secondary hypertriglyceridemia 		1 0 1 0.50 0 0
CUI: C1096710
Disease: Lactescent serum
Lactescent serum 		1 0 1 0.50 0 0
CUI: C1969232
Disease: HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11 		1 0 1 0.50 0 0
CUI: C4017648
Disease: LPL-ARITA PHENOTYPE
LPL-ARITA PHENOTYPE 		1 0 1 0.50 0 0
CUI: C4017649
Disease: LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE
LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE 		1 0 1 0.50 0 0
CUI: C4703544
Disease: Elevated apolipoprotein B level
Elevated apolipoprotein B level 		1 0 1 0.50 0 0
CUI: C4703546
Disease: Elevated apolipoprotein A-II level
Elevated apolipoprotein A-II level 		1 0 1 0.50 0 0
CUI: C2931862
Disease: Familial hyperchylomicronemia syndrome
Familial hyperchylomicronemia syndrome 		5 0 2 0.40 0 0
CUI: C0151465
Disease: Renal abscess
Renal abscess 		2 0 1 0.33 0 0
CUI: C0151826
Disease: Retrosternal pain
Retrosternal pain 		2 0 1 0.33 0 0
CUI: C0268197
Disease: Familial lipoprotein deficiency
Familial lipoprotein deficiency 		2 0 1 0.33 0 0
CUI: C0278836
Disease: Stage III Prostate Carcinoma
Stage III Prostate Carcinoma 		2 0 1 0.33 0 0
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 0.33 0 0
CUI: C1261969
Disease: Type I hyperlipidaemia
Type I hyperlipidaemia 		2 0 1 0.33 0 0
CUI: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia 		2 0 1 0.33 0 0
CUI: C1855498
Disease: Lipase deficiency combined
Lipase deficiency combined 		2 0 1 0.33 0 0
CUI: C3889891
Disease: APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE
APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE 		2 0 1 0.33 0 0
CUI: C4016424
Disease: HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO
HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO 		2 0 1 0.33 0 0
CUI: C4017134
Disease: APOLIPOPROTEIN C-II (PARIS) PHENOTYPE
APOLIPOPROTEIN C-II (PARIS) PHENOTYPE 		2 0 1 0.33 0 0
CUI: C4017135
Disease: APOLIPOPROTEIN C-II (BARI) PHENOTYPE
APOLIPOPROTEIN C-II (BARI) PHENOTYPE 		2 0 1 0.33 0 0
CUI: C4017136
Disease: APOLIPOPROTEIN C-II VARIANT PHENOTYPE
APOLIPOPROTEIN C-II VARIANT PHENOTYPE 		2 0 1 0.33 0 0