LPL, lipoprotein lipase, 4023

N. diseases: 290; N. variants: 116
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0342889
Disease: Secondary hypertriglyceridemia
Secondary hypertriglyceridemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 1 0.020 None 1.000 2 1973 2003
CUI: C1096710
Disease: Lactescent serum
Lactescent serum 		phenotype Finding 1 0.100 None 0
CUI: C1969232
Disease: HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4017648
Disease: LPL-ARITA PHENOTYPE
LPL-ARITA PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4017649
Disease: LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE
LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4703544
Disease: Elevated apolipoprotein B level
Elevated apolipoprotein B level 		phenotype Finding 1 0.100 None 0
CUI: C4703546
Disease: Elevated apolipoprotein A-II level
Elevated apolipoprotein A-II level 		phenotype Finding 1 0.100 None 0
CUI: C1261969
Disease: Type I hyperlipidaemia
Type I hyperlipidaemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 1 0.050 None 1.000 5 1 1992 2014
CUI: C1274228
Disease: Chylomicronemia syndrome
Chylomicronemia syndrome 		disease Disease or Syndrome 2 0.040 None 1.000 4 1990 2013
CUI: C0151465
Disease: Renal abscess
Renal abscess 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Acquired Abnormality 2 0.010 None 1.000 1 2015 2015
CUI: C0151826
Disease: Retrosternal pain
Retrosternal pain 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Sign or Symptom 2 7 0.010 None 1.000 1 3 1998 1998
CUI: C0268197
Disease: Familial lipoprotein deficiency
Familial lipoprotein deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1997 1997
CUI: C0278836
Disease: Stage III Prostate Carcinoma
Stage III Prostate Carcinoma 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 2 0.010 None 1.000 1 1999 1999
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		disease Nutritional and Metabolic Diseases Congenital Abnormality 2 0.010 None 1.000 1 1989 1989
CUI: C1855498
Disease: Lipase deficiency combined
Lipase deficiency combined 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 2 0.010 None 1.000 1 2007 2007
CUI: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia 		phenotype Nutritional and Metabolic Diseases Finding 2 2 0.100 None 0 2
CUI: C4016424
Disease: HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO
HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO 		phenotype Finding 2 3 0.100 None 0 1
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 5 0.320 None 0.500 2 2001 2007
CUI: C0020481
Disease: Hyperlipoproteinemia Type V
Hyperlipoproteinemia Type V 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 3 0.010 None 1.000 1 2005 2005
CUI: C1291447
Disease: Deficiency of triacylglycerol lipase
Deficiency of triacylglycerol lipase 		disease Disease or Syndrome 3 0.010 None 1.000 1 1988 1988
CUI: C0221252
Disease: Eruptive xanthoma
Eruptive xanthoma 		disease Nutritional and Metabolic Diseases Disease or Syndrome 4 1 0.110 None 1.000 1 2014 2014
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 4 2 0.010 None 1.000 1 2014 2014
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis 		disease Eye Diseases Disease or Syndrome 4 0.100 None 0
CUI: C2931862
Disease: Familial hyperchylomicronemia syndrome
Familial hyperchylomicronemia syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 2 0.050 None 1.000 5 2 1991 2017
CUI: C4021729
Disease: Increased VLDL cholesterol concentration
Increased VLDL cholesterol concentration 		phenotype Nutritional and Metabolic Diseases Finding 5 0.100 None 0