2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Other Metabolic Disorders And Immunity Disorders 270-279 > Disorders Of Lipoid Metabolism 272.* >  2008 ICD-9-CM Diagnosis 272.3
Hyperchylomicronemia- A rare familial condition characterized by massive chylomicronemia and decreased levels of other lipoproteins. It is due to deficiency of lipoprotein lipase, an alkaline triglyceride hydrolase which catalyzes an important step in the extrahepatic removal of triglyceride-rich lipoproteins from the blood.
- 272.3 is a specific code that can be used to specify a diagnosis
- 272.3 contains 18 index entries
- View the ICD-9-CM Volume 1 272.* hierarchy
272.3 also known as:- Bürger-Grütz syndrome
- Fredrickson type I or V hyperlipoproteinemia
- Hyperlipidemia, Group D
- Mixed hyperglyceridemia
Index entries containing 272.3:- Bürger-Grütz disease or syndrome (essential familial hyperlipemia)
 272.3
Chylomicronemia (fasting) (with hyperprebetalipoproteinemia) 272.3
Disease, diseased - see also Syndrome- Bürger-Grütz (essential familial hyperlipemia) 272.3
Hepatosplenomegaly 571.8- hyperlipemic (Bürger-Grutz type) 272.3
Hyperchylomicronemia (familial) (with hyperbetalipoproteinemia) 272.3
Hyperglyceridemia 272.1- mixed 272.3
Hyperlipidemia 272.4- exogenous 272.3
- fat-induced 272.3
- group
- D 272.3
Hyperlipoproteinemia (acquired) (essential) (familial) (hereditary) (primary) (secondary) 272.4- Fredrickson type
- I 272.3
- V 272.3
Hyperprebetalipoproteinemia 272.1- with chylomicronemia 272.3
Lipemia (see also Hyperlipidemia) 272.4- retina, retinalis 272.3
Lipidosis 272.7- hepatosplenomegalic 272.3
Prebetalipoproteinemia (acquired) (essential) (familial) (hereditary) (primary) (secondary) 272.1- with chylomicronemia 272.3
Syndrome - see also Disease- Bürger-Grutz (essential familial hyperlipemia) 272.3
Xanthoma(s), xanthomatosis 272.2- with
- hyperlipoproteinemia
- type I 272.3
- type V 272.3
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