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
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
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: C0022346
Disease: Icterus
Icterus
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 241 17 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
CUI: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia
phenotype Nutritional and Metabolic Diseases Finding 2 2 0.100 None 0 2
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased
phenotype Nutritional and Metabolic Diseases Finding 23 318 0.100 None 0
CUI: C0027497
Disease: Nausea
Nausea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 161 14 0.100 None 0 2
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: C0042963
Disease: Vomiting
Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 303 23 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: C4703546
Disease: Elevated apolipoprotein A-II level
Elevated apolipoprotein A-II level
phenotype Finding 1 0.100 None 0
CUI: C1096710
Disease: Lactescent serum
Lactescent serum
phenotype Finding 1 0.100 None 0
CUI: C4703544
Disease: Elevated apolipoprotein B level
Elevated apolipoprotein B level
phenotype Finding 1 0.100 None 0
Increased VLDL cholesterol concentration
phenotype Nutritional and Metabolic Diseases Finding 5 0.100 None 0
Deficiency of triacylglycerol lipase
disease Disease or Syndrome 3 0.010 None 1.000 1 1988 1988
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia
disease Nutritional and Metabolic Diseases Congenital Abnormality 2 0.010 None 1.000 1 1989 1989
CUI: C0239981
Disease: Hypoalbuminemia
Hypoalbuminemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 107 9 0.010 None 1.000 1 1991 1991
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders Disease or Syndrome 978 115 0.010 None 1.000 1 1991 1991
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
group Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 2780 385 0.010 None 1.000 1 1994 1994
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
group Digestive System Diseases Disease or Syndrome 1577 605 0.010 None 1.000 1 1994 1994
CUI: C0001206
Disease: Acromegaly
Acromegaly
disease Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 138 25 0.010 None 1.000 1 1995 1995
CUI: C1504375
Disease: Diabetic macroangiopathy
Diabetic macroangiopathy
disease Disease or Syndrome 9 2 0.010 None 1.000 1 1995 1995