Secondary hypertriglyceridemia
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
1
|
|
0.020 |
None |
1.000 |
2 |
|
1973 |
2003 |
Lactescent serum
|
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
|
|
|
LPL-ARITA PHENOTYPE
|
phenotype |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
LIPOPROTEIN LIPASE (OLBIA) PHENOTYPE
|
phenotype |
|
Finding
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Elevated apolipoprotein B level
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Elevated apolipoprotein A-II level
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
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 |
Chylomicronemia syndrome
|
disease |
|
Disease or Syndrome
|
2
|
|
0.040 |
None |
1.000 |
4 |
|
1990 |
2013 |
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 |
Retrosternal pain
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Sign or Symptom
|
2
|
7
|
0.010 |
None |
1.000 |
1 |
3
|
1998 |
1998 |
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 |
Stage III Prostate Carcinoma
|
disease |
Neoplasms; Male Urogenital Diseases
|
Neoplastic Process
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Primary hypertriglyceridemia
|
disease |
Nutritional and Metabolic Diseases
|
Congenital Abnormality
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
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 |
Hyperchylomicronemia
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
2
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO
|
phenotype |
|
Finding
|
2
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
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 |
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 |
Deficiency of triacylglycerol lipase
|
disease |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
1988 |
1988 |
Eruptive xanthoma
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
4
|
1
|
0.110 |
None |
1.000 |
1 |
|
2014 |
2014 |
Recurrent abdominal pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
4
|
2
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Lipidemia retinalis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
4
|
|
0.100 |
None |
|
0 |
|
|
|
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 |
Increased VLDL cholesterol concentration
|
phenotype |
Nutritional and Metabolic Diseases
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|