5C80.2ICD-11 MMS 2026-01
Mixed hyperlipidaemia
Description
Elevated levels of both LDL cholesterol and triglycerides in the blood
Index terms
- Mixed hyperlipidaemia
- Hyperbetalipoproteinaemia with prebetalipoproteinaemia
- Hypercholesterolaemia with endogenous hyperglyceridaemia
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- Hyperlipidaemia, group C
- familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia
- familial hypercholesterolaemia with hyperlipaemia
- mixed hyperlipemia
- prebetalipoproteinemia hyperbetalipoproteinaemia
- remnant hyperlipoproteinemia
- Hyperlipidaemia type 3
- Broad beta disease
- Broad- or floating-betalipoproteinaemia
- Broad-betalipoproteinaemia
- Familial type 3 hyperlipoproteinaemia
- Fredrickson type 3 hyperlipoproteinaemia
- Hyperlipoproteinaemia type 3
- Remnant hyperlipidaemia
- broad-beta lipoproteinemia
- floating beta disease
- floating-beta lipoproteinemia
- Hyperlipidaemia type 3 - Apolipoprotein E deficiency
- apolipoprotein E deficiency
- Hyperlipidaemia type 3 - familial defective apolipoprotein B
- Hyperlipidaemia type 3 - familial dysbetalipoproteinaemia
- Familial dysbetalipoproteinaemia
- dysbetalipoproteinaemia
- primary dysbetalipoproteinaemia
- Hyperlipidaemia type 3 - familial dyslipoproteinaemia
- Secondary hyperlipoproteinaemia type 3
- Mixed hyperlipidaemia - type IIb hyperlipoproteinaemia
- Fredrickson type 2B hyperlipoproteinemia
- familial hyperlipoproteinemia type 2B
- Familial combined hyperlipidaemia
- FCH - [familial combined hyperlipidaemia]
- hyperapobetalipoproteinaemia
- Secondary combined hyperlipidaemia
- Mixed hyperlipidaemia due to hepatic triglyceride lipase deficiency
- Xanthoma in association with primary combined hyperlipidaemia
- Xanthoma in association with secondary hyperlipidaemia
Inclusions
- Hyperbetalipoproteinaemia with prebetalipoproteinaemia
- Hypercholesterolaemia with endogenous hyperglyceridaemia
- Hyperlipidaemia, group C
Excludes
5C52.11– cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]
Exclusions from above levels
5C56.0– Sphingolipidosis3A10.Z– Hereditary haemolytic anaemia due to enzyme deficiency5A71.01– Congenital adrenal hyperplasia
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Sibling codes
Foundation entity
Mixed hyperlipidaemia – http://id.who.int/icd/entity/405028062
Allowed postcoordination axes
Part of: 5C80: Hyperlipoproteinaemia › 05: Endocrine, nutritional or metabolic diseases