APOA5, apolipoprotein A5, 116519

N. diseases: 107; N. variants: 22
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.
HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
phenotype Finding 1 3 0.100 None 0 3
Increased VLDL cholesterol concentration
phenotype Nutritional and Metabolic Diseases Finding 5 0.100 None 0
CUI: C4025807
Disease: Atheroeruptive xanthoma
Atheroeruptive xanthoma
disease Nutritional and Metabolic Diseases Disease or Syndrome 1 0.100 None 0
Decreased HDL cholesterol concentration
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Finding 12 2 0.100 None 0
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 596 81 0.100 None 0
Decreased LDL cholesterol concentration
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Finding 9 0.100 None 0
CUI: C0813230
Disease: Serum triglycerides increased
Serum triglycerides increased
phenotype Nutritional and Metabolic Diseases Finding 5 6 0.100 None 0 1
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 69 4 0.100 None 0
CUI: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia
phenotype Nutritional and Metabolic Diseases Finding 2 2 0.100 None 0
CUI: C4021654
Disease: Precocious atherosclerosis
Precocious atherosclerosis
phenotype Cardiovascular Diseases Pathologic Function 9 0.100 None 0
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 191 67 0.300 None 1.000 1 2014 2014
CUI: C4704956
Disease: Adolescent Overweight
Adolescent Overweight
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4704955
Disease: Infant Overweight
Infant Overweight
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4317171
Disease: Adolescent Obesity
Adolescent Obesity
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 18 9 0.300 None 1.000 1 2014 2014
CUI: C4521075
Disease: Childhood Overweight
Childhood Overweight
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Finding 4 0.300 None 1.000 1 2014 2014
CUI: C4553478
Disease: Infantile Obesity
Infantile Obesity
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 5 0.300 None 1.000 1 2014 2014
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 613 283 0.200 None 1.000 1 2005 2005
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
phenotype Laboratory Procedure 39 568 0.100 None 1.000 1 1 2011 2011
CUI: C0162701
Disease: Polysomnography
Polysomnography
phenotype Diagnostic Procedure 119 249 0.100 None 1.000 1 2 2012 2012
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
phenotype Laboratory or Test Result 269 549 0.100 None 1.000 1 1 2018 2018
Low density lipoprotein cholesterol measurement
phenotype Laboratory Procedure 483 1142 0.100 None 1.000 1 2 2018 2018
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
group Laboratory Procedure 27 53 0.100 None 1.000 1 1 2012 2012
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
phenotype Laboratory Procedure 433 3282 0.100 None 1.000 1 4 2012 2012
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
phenotype Laboratory Procedure 283 679 0.100 None 1.000 1 7 2012 2012
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
phenotype Laboratory Procedure 138 216 0.100 None 1.000 1 1 2018 2018