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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 272.1 Pure hyperglyceridemia  On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date. The 2009 version of ICD-9-CM 272.1 can be accessed here. A familial disorder characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in VLDL. It is considered to be an autosomal dominant trait. 272.1 is a specific code that can be used to specify a diagnosis 272.1 contains 20 index entries View the ICD-9-CM Volume 1 272.* hierarchy 272.1 also known as: Endogenous hyperglyceridemia Fredrickson Type IV hyperlipoproteinemia Hyperlipidemia, Group B Hyperprebetalipoproteinemia Hypertriglyceridemia, essential Very-low-density-lipoid-type [VLDL] hyperlipoproteinemia Index entries containing 272.1: Elevation triglycerides 272.1 with cholesterol 272.2 Findings, abnormal, without diagnosis (examination) (laboratory test) 796.4 triglycerides 272.9 high 272.1 with high cholesterol 272.2 High triglycerides 272.1 with high cholesterol 272.2 Hyperglyceridemia 272.1 endogenous 272.1 essential 272.1 familial 272.1 hereditary 272.1 mixed 272.3 pure 272.1 Hyperlipidemia 272.4 carbohydrate-induced 272.1 endogenous 272.1 group B 272.1 Hyperlipoproteinemia (acquired) (essential) (familial) (hereditary) (primary) (secondary) 272.4 Fredrickson type IV 272.1 very-low-density-lipoid-type [VLDL] 272.1 Hyperprebetalipoproteinemia 272.1 with chylomicronemia 272.3 familial 272.1 Hypertriglyceridemia, essential 272.1 Lipoproteinemia (alpha) 272.4 hyper-pre-beta 272.1 Prebetalipoproteinemia (acquired) (essential) (familial) (hereditary) (primary) (secondary) 272.1 with chylomicronemia 272.3 Xanthoma(s), xanthomatosis 272.2 with hyperlipoproteinemia type IV 272.1