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.
LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C3808022
Disease: Episodic abdominal pain
Episodic abdominal pain
phenotype Pathological Conditions, Signs and Symptoms Finding 39 3 0.100 None 0 2
CUI: C0027497
Disease: Nausea
Nausea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 161 14 0.100 None 0 2
HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO
phenotype Finding 2 3 0.100 None 0 1
CUI: C4017648
Disease: LPL-ARITA PHENOTYPE
LPL-ARITA PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased
phenotype Nutritional and Metabolic Diseases Finding 23 318 0.100 None 0
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases Sign or Symptom 127 21 0.100 None 0
Increased VLDL cholesterol concentration
phenotype Nutritional and Metabolic Diseases Finding 5 0.100 None 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis
disease Eye Diseases Disease or Syndrome 4 0.100 None 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
CUI: C0022346
Disease: Icterus
Icterus
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 241 17 0.100 None 0
CUI: C1096710
Disease: Lactescent serum
Lactescent serum
phenotype Finding 1 0.100 None 0
CUI: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 0.100 None 0 2
CUI: C4703546
Disease: Elevated apolipoprotein A-II level
Elevated apolipoprotein A-II level
phenotype Finding 1 0.100 None 0
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
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: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia
phenotype Nutritional and Metabolic Diseases Finding 2 2 0.100 None 0 2
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: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 340 169 0.600 None 0.988 169 11 1975 2019
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 36 64 1.000 strong 0.993 153 55 1977 2019
CUI: C0020480
Disease: Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type IV
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 11 3 0.190 None 0.889 9 1 1977 2017
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.100 None 0.909 11 1985 2017
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 91 28 0.800 strong 1.000 30 6 1987 2020
Deficiency of triacylglycerol lipase
disease Disease or Syndrome 3 0.010 None 1.000 1 1988 1988
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 472 83 0.700 None 0.952 21 2 1989 2019