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: C4703546
Disease: Elevated apolipoprotein A-II level
Elevated apolipoprotein A-II level
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: C0022346
Disease: Icterus
Icterus
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 241 17 0.100 None 0
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11
phenotype Finding 1 1 0.100 None 0 1
CUI: C1096710
Disease: Lactescent serum
Lactescent serum
phenotype Finding 1 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: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis
disease Eye Diseases Disease or Syndrome 4 0.100 None 0
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased
phenotype Nutritional and Metabolic Diseases Finding 23 318 0.100 None 0
CUI: C3808022
Disease: Episodic abdominal pain
Episodic abdominal pain
phenotype Pathological Conditions, Signs and Symptoms Finding 39 3 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: C4703544
Disease: Elevated apolipoprotein B level
Elevated apolipoprotein B level
phenotype Finding 1 0.100 None 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 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
Increased VLDL cholesterol concentration
phenotype Nutritional and Metabolic Diseases Finding 5 0.100 None 0
LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
phenotype Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 186 43 0.020 None < 0.001 2 2006 2011
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
Polypoidal choroidal vasculopathy
disease Disease or Syndrome 56 67 0.020 None < 0.001 2 2015 2018
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6385 327 0.010 None < 0.001 1 2006 2006
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic
disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 61 86 0.010 None < 0.001 1 2008 2008
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension
disease Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 52 22 0.010 None < 0.001 1 2006 2006
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
group Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2492 85 0.010 None < 0.001 1 2006 2006
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 34 5 0.010 None < 0.001 1 2017 2017
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
phenotype Pathological Conditions, Signs and Symptoms Neoplastic Process 3865 72 0.010 None < 0.001 1 2019 2019