APOC3, apolipoprotein C3, 345

N. diseases: 153; N. variants: 15
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: C0178874
Disease: Tumor Progression
Tumor Progression
phenotype Pathological Conditions, Signs and Symptoms Neoplastic Process 3865 72 0.010 None 1.000 1 2016 2016
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina
disease Cardiovascular Diseases Disease or Syndrome 39 10 0.010 None 1.000 1 2001 2001
CUI: C0596848
Disease: lipoprotein disorder
lipoprotein disorder
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 1992 1992
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 4081 1204 0.010 None 1.000 1 1999 1999
CUI: C0702166
Disease: Acne
Acne
disease Skin and Connective Tissue Diseases Disease or Syndrome 167 11 0.010 None 1.000 1 2014 2014
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 18 6 0.010 None 1.000 1 1986 1986
CUI: C1858501
Disease: Spinocerebellar Ataxia 12
Spinocerebellar Ataxia 12
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2012 2012
CUI: C2609253
Disease: Macrovascular disease
Macrovascular disease
disease Disease or Syndrome 23 1 0.010 None 1.000 1 2005 2005
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia
disease Disease or Syndrome 17 4 0.010 None 1.000 1 2017 2017
CUI: C2936179
Disease: Obesity, Visceral
Obesity, Visceral
phenotype Nutritional and Metabolic Diseases Sign or Symptom 55 3 0.010 None 1.000 1 2012 2012
CUI: C3160761
Disease: Diabetic dyslipidaemia
Diabetic dyslipidaemia
disease Disease or Syndrome 28 11 0.010 None 1.000 1 2019 2019
CUI: C3665335
Disease: Cutis laxa, autosomal recessive
Cutis laxa, autosomal recessive
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2009 2009
Arteriosclerotic cardiovascular disease, NOS
disease Cardiovascular Diseases Disease or Syndrome 58 5 0.010 None 1.000 1 2019 2019
CUI: C4016282
Disease: BREAST CANCER, SOMATIC
BREAST CANCER, SOMATIC
disease Neoplastic Process 4 1 0.010 None 1.000 1 1999 1999
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 2016 2016
CUI: C4476910
Disease: Thin-cap fibroatheroma
Thin-cap fibroatheroma
phenotype Cardiovascular Diseases Acquired Abnormality 12 0.010 None 1.000 1 2018 2018
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.010 None < 0.001 1 2011 2011
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 50 15 0.010 None < 0.001 1 2019 2019
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
Classical Hodgkin's Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 285 20 0.010 None 1.000 1 2002 2002
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 196 76 0.010 None 1.000 1 2004 2004
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
phenotype Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 186 43 0.010 None 1.000 1 2007 2007
CUI: C0854441
Disease: Gastric mucosal lesion
Gastric mucosal lesion
disease Disease or Syndrome 4 0.010 None 1.000 1 2015 2015
CUI: C0856151
Disease: Fat redistribution
Fat redistribution
phenotype Disease or Syndrome 12 0.010 None 1.000 1 2007 2007
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2016 2016
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2020 2020