APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
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: C3875011
Disease: Familial hyperalphalipoproteinemia
Familial hyperalphalipoproteinemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 5 0.010 None 1.000 1 1993 1993
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: C0264683
Disease: Coronary artery atheroma
Coronary artery atheroma 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 6 0.020 None 1.000 2 2005 2019
CUI: C1862968
Disease: Generalized amyloid deposition
Generalized amyloid deposition 		phenotype Nutritional and Metabolic Diseases Finding 6 0.100 None 0
CUI: C0334265
Disease: Transitional Cell Neoplasm
Transitional Cell Neoplasm 		disease Neoplasms Neoplastic Process 7 0.200 None 1.000 1 2009 2009
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 8 15 0.700 None 1.000 8 5 1988 2019
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		disease Disease or Syndrome 8 4 0.300 limited 1.000 1 1999 1999
CUI: C0023195
Disease: Lecithin Acyltransferase Deficiency
Lecithin Acyltransferase Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 22 0.030 None 1.000 3 1981 2019
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		disease Disease or Syndrome 9 4 0.020 None 1.000 2 1990 2009
CUI: C0042929
Disease: Polyp of vocal cord
Polyp of vocal cord 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Neoplastic Process 9 0.010 None 1.000 1 2017 2017
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
Amyloidosis, Primary Cutaneous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 9 10 0.010 None 1.000 1 1 1999 1999
CUI: C2931838
Disease: Familial HDL deficiency
Familial HDL deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 1 0.050 None 1.000 5 1991 2016
CUI: C0795956
Disease: Chylomicron retention disease
Chylomicron retention disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 10 6 0.010 None 1.000 1 2012 2012
CUI: C1720452
Disease: Soft drusen
Soft drusen 		disease Disease or Syndrome 10 5 0.010 None 1.000 1 2019 2019
CUI: C4081731
Disease: Hereditary systemic amyloidosis
Hereditary systemic amyloidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 6 0.010 None 1.000 1 2008 2008
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 0.030 None 1.000 3 1987 2007
CUI: C0151691
Disease: Decreased HDL cholesterol concentration
Decreased HDL cholesterol concentration 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Finding 12 2 0.100 None 0
CUI: C1704378
Disease: Heymann Nephritis
Heymann Nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 13 0.300 None 1.000 1 1995 1995
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 15 16 0.010 None 1.000 1 1993 1993
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		disease Disease or Syndrome 17 4 0.020 None 1.000 2 1999 2005
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 18 6 0.560 strong 1.000 9 1986 2016
CUI: C0685889
Disease: Splenic Hypoplasia
Splenic Hypoplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Congenital Abnormality 18 9 0.010 None 1.000 1 2019 2019
CUI: C1536221
Disease: Non ST segment elevation myocardial infarction
Non ST segment elevation myocardial infarction 		disease Disease or Syndrome 18 0.010 None 1.000 1 2019 2019
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
Ataxia with vitamin E deficiency 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 32 0.300 None 1.000 1 2008 2008
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