Disorders Of Lipoprotein Metabolism Or Certain Specified Lipidaemias – Definitions & ICD 11 Codes


Exclusions:

Coded Elsewhere:


  • Lipoid dermatoarthritis (FA38.Y)
  • Multicentric reticulohistiocytosis (EE8Y)
  • Lipoid proteinosis (LD27.Y)

Hyperlipoproteinaemia

Definition of Hyperlipoproteinaemia: Disorders of lipoprotein metabolism that result in high levels of lipoproteins in the circulating blood

  5C80  Hyperlipoproteinaemia

5C80.0 Hypercholesterolaemia

5C80.00 Primary hypercholesterolaemia

Definition of Primary hypercholesterolaemia: 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.

Coded Elsewhere:

  • Sitosterolaemia (5C52.1Y)

5C80.01 Secondary hypercholesterolaemia

Coding Note:

  • Code also the causing condition

5C80.0Z Hypercholesterolaemia unspecified

5C80.1 Hypertriglyceridaemia

Definition of Hypertriglyceridaemia: A form of hyperlipidaemia characterised by abnormally elevated levels of triglyceride-rich lipoproteins in the blood. It is associated with an elevated risk of cardiovascular morbidity.

Inclusions:

  • Hyperlipidaemia, group B
  • Endogenous hyperglyceridaemia

5C80.2 Mixed hyperlipidaemia

Definition of Mixed hyperlipidaemia: Elevated levels of both LDL cholesterol and triglycerides in the blood

Inclusions:

  • Hyperbetalipoproteinaemia with prebetalipoproteinaemia
  • Hypercholesterolaemia with endogenous hyperglyceridaemia
  • Hyperlipidaemia, group C

Exclusions:

  • cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein] (5C52.11)

5C80.3 Hyperalphalipoproteinaemia

Definition of Hyperalphalipoproteinaemia: A condition in which high-density lipoprotein is elevated in the blood.

5C80.Y Other specified hyperlipoproteinaemia

5C80.Z Hyperlipoproteinaemia unspecified

Hypolipoproteinaemia

Definition of Hypolipoproteinaemia: Disorders characterised by low level of lipoproteins of any type in the blood

ICD 11 Code For Hypolipoproteinaemia

  5C81  Hypolipoproteinaemia

Inclusions:

  • High-density lipoprotein deficiency

5C81.0 Hypoalphalipoproteinaemia

Definition of Hypoalphalipoproteinaemia: A disorder characterised by low levels of high-density lipoprotein in the blood.

5C81.1 Hypobetalipoproteinaemia

Definition of Hypobetalipoproteinaemia: Hypobetalipoproteinemia (HBL) constitutes a group of lipoprotein metabolism disorders that are characterised by permanently low levels (below the 5th percentile) of apolipoprotein B and LDL cholesterol. There are two types of HBL: familial hypobetalipoproteinemia and chylomicron retention disease (CMRD; see these terms). The familial form can be severe with early onset (abetalipoproteinemia/homozygous familial hypobetalipoproteinemia; see this term) or benign (benign familial hypobetalipoproteinemia; see this term). (Please add the sentence). Severe familial HBL and CMRD appear in infancy or childhood. As a result they are often associated with growth delay, diarrhoea with steatorrhoea, and fat malabsorption. Benign familial hypobetalipoproteinemia is generally asymptomatic, but in adults is occasionally associated with dietary intolerance to fat. HBL disorders are caused by mutations in proteins involved in the synthesis, secretion and catabolism of lipoproteins containing apolipoprotein B (LDL, VLDL and chylomicrons).

5C81.Y Other specified hypolipoproteinaemia

5C81.Z Hypolipoproteinaemia unspecified

Other specified disorders of lipoprotein metabolism or lipidaemias

ICD 11 Code For Other specified disorders of lipoprotein metabolism or lipidaemias

  5C8Y  Other specified disorders of lipoprotein metabolism or lipidaemias

Unspecified disorders of lipoprotein metabolism or lipidaemias

ICD 11 Code For Unspecified disorders of lipoprotein metabolism or lipidaemias

  5C8Z  Unspecified disorders of lipoprotein metabolism or lipidaemias

Metabolic or transporter liver disease

ICD 11 Code For Metabolic or transporter liver disease

  5C90  Metabolic or transporter liver disease

Exclusions:

  • Alcoholic liver disease (DB94)
  • Non-alcoholic fatty liver disease (DB92)
  • Drug-induced or toxic liver disease (DB95)
  • Acute fatty liver of pregnancy (JA65.0)

Coded Elsewhere:

5C90.0 Liver diseases due to urea cycle defects

Definition of Liver diseases due to urea cycle defects: This is a group of liver diseases due to defects in the urea cycle, which is a metabolic cycle of nitrogen-containing compounds that produces the waste product urea.

Coded Elsewhere:

5C90.1 Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport

Definition of Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport: These are liver diseases due to disorders of porphyrin and bilirubin metabolism and transport

Exclusions:

  • Defects of catalase and peroxidase (5C58)

Coded Elsewhere:

5C90.2 Liver diseases due to disorders of amino acid metabolism

Definition of Liver diseases due to disorders of amino acid metabolism: This is liver disease due to the disorder of the various biochemical processes responsible for the synthesis of proteins and amino acids, and the breakdown of proteins (and other large molecules, too) by catabolism.

Coded Elsewhere:

5C90.3 Liver disease due to disorders of lysosomal storage

Definition of Liver disease due to disorders of lysosomal storage: This is liver disease due to a group of approximately 50 rare inherited metabolic disorders that result from defects in lysosomal function.

Coded Elsewhere:

  • Gaucher disease (5C56.0Y)
  • Niemann-Pick disease (5C56.0Y)
  • Wolman disease (5C56.0Y)
  • Cholesteryl ester storage disease (5C56.0Y)

5C90.4 Liver diseases due to mitochondrial disorders

Definition of Liver diseases due to mitochondrial disorders: This is liver disease due to a group of disorders caused by dysfunctional mitochondria, the organelles that generate energy for the cell.

5C90.5 Liver diseases due to disorders of mineral metabolism

Definition of Liver diseases due to disorders of mineral metabolism: This is a liver disease due to a disorder of the organic compound required by an organism as a vital nutrient in limited amounts.

Coding Note:

  • Code also the causing condition

5C90.Y Other specified metabolic or transporter liver disease

5C90.Z Metabolic or transporter liver disease unspecified

Similar Posts

Leave a Reply

Your email address will not be published. Required fields are marked *