
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Hypercholesterolemia causes
Introduction
Overview
Overview
Hypercholesterolemia is primarily caused by cardiovascular conditions resulting from lifestyle, renal disease, and congenital conditions.
Causes
Causes
Common Causes
- AbetalipoproteinemiÂ
- Alagille syndrome
- ApoA1 deficiency
- Apob mutation
- Apolipoprotein c-ii deficiency
- Apoprotein e deficiency
- Beckwith-wiedemann syndrome
- Beta blockers
- Carbohydrate intake
- Cholestatic jaundice
- Chronic renal insufficiency
- Ciclosporin
- Cushing’s syndrome
- Diabetes mellitus
- Diabetes mellitus type 2
- Dialysis
- Familial defective apolipoprotein b-100
- Familial mixed hyperlipidaemia
- Hypothyroidism
- Idiopathic
- Lack of exercise
- Lack of physical activity
- Ldl receptor deficiency
- Ldlr mutation
- Ldlrap1 mutation
- Lipoprotein lipase deficiency
- Malignant hepatopathy
- Metabolic syndrome
- Monoclonal gammopathy
- Nephrotic syndrome
- Obesity
- Obstructive liver disease
- Oculomotor apraxia syndrome
- Pcsk9 mutation
- Tobacco
- Trans fatty acids
- Vitamin e deficiency
Causes by Organ System
Causes in Alphabetical Order
- AbetalipoproteinemiaÂ
- Alagille syndrome
- Alcohol
- Alström syndrome
- Analbuminaemia
- Anorexia nervosa
- ApoA1 deficiency
- Apob mutation
- Apolipoprotein c-ii deficiency
- Apoprotein e deficiency
- Beckwith-wiedemann syndrome
- Beta blockers
- Carbohydrate intake
- Carcinoma
- Cholestatic jaundice
- Cholesterol ester storage disease
- Chromosome 14 uniparental disomy syndromeÂ
- Chromosome 3, trisomy 3p
- Chronic renal insufficiency
- Ciclosporin
- Cushing’s syndrome
- Cushing’s syndrome
- Diabetes mellitus
- Diabetes mellitus type 2
- Dialysis
- Familial
- Familial defective apolipoprotein b-100
- Familial mixed hyperlipidaemia
- Fosamprenavir
- Glucocorticoids
- Glycogenosis type 1a
- Glycogenosis type 3
- Glycogenosis type 6
- Hypothyroidism
- Idiopathic
- Lack of exercise
- Lack of physical activity
- Ldl receptor deficiency
- Ldlr mutation
- Ldlrap1 mutation
- Lipoprotein lipase deficiency
- Malignant hepatopathy
- Medications
- Metabolic syndrome
- Mitotane
- Monoclonal gammopathy
- Nephrotic syndrome
- Obesity
- Obstructive liver disease
- Oculomotor apraxia syndrome
- Pcsk9 mutation
- Pregnancy
- Retinoic acid
- Siltuximab
- Sirolimus
- Temsirolimus
- Thiazide diuretics
- Tobacco
- Tocilizumab
- Tofacitinib
- Trans fatty acids
- Vitamin e deficiency
- Werner syndrome
- Zieve’s syndrome
References
References
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Luke Rusowicz-Orazem, B.S.
