5C80.00 Primary hypercholesterolaemia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
This is a genetic disorder characterised by high cholesterol levels, specifically very high levels of low-density lipoprotein (LDL, "bad cholesterol"), in the blood and early cardiovascular disease.
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synonyms
- Primary hypercholesterolaemia
- low-density-lipoid-type hyperlipoproteinemia
- pure hypercholesterolaemia
- LDL - [low density lipoprotein} hyperlipoproteinemia
- group A hyperlipidaemia
- pure hypercholesterinaemia
- cholesterolaemia
- essential cholesterolaemia
- essential hypercholesterolaemia
- group A hyperlipemia
- increased low density lipoprotein
- low-density-lipoprotein-type
- low-density-lipoprotein-type hyperlipoproteinemia
- Familial hypercholesterolaemia
- Hypercholesterolaemia due to LDL receptor deficiency
- low density lipoprotein catabolic defect
- low density lipoprotein receptor disorder
- familial hypercholesterinaemia
- essential familial hypercholesterolaemia
- hereditary cholesterolaemia
- hereditary hypercholesterinaemia
- hereditary hypercholesterolaemia
- familial hyperbetalipoproteinaemia
- Fredrickson 2A
- Fredrickson type 2A hyperlipoproteinemia
- familial cholesterolaemia
- Familial hypercholesterolaemia - heterozygous
- Familial hypercholesterolaemia - homozygous
- Familial hypercholesterolemic xanthomatosis
- Familial defective apolipoprotein B-100
- Autosomal recessive hypercholesterolaemia
- Autosomal dominant hypercholesterolaemia
- Polygenic hypercholesterolaemia
- Hyperbetalipoproteinaemia
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