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.

code elsewhere

• Sitosterolaemia  (5C52.1Y)

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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