Elevated fasting triglycerides
Endogenous hyperglyceridemia
Fredrickson’s hyperlipoproteinemia, type IV
Hyperlipidemia, group B
Hyperprebetalipoproteinemia
Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinemia
Hyperlipoproteinemia, type i
Hypertriglyceridemia
Hypertriglyceridemia high blood fats)
Hypertriglyceridemia, endogenous
Hypertriglyceridemia, primary
Primary hypertriglyceridemia
A hypertriglyceridemia disorder, often with autosomal dominant inheritance. It is characterized by the persistent elevations of plasma triglycerides, endogenously synthesized and contained predominantly in very-low-density lipoproteins pre-beta lipoproteins). In contrast, the plasma cholesterol and phospholipids usually remain within normal limits.
Characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in vldl; considered to be an autosomal dominant trait.
E78.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM E78.1 became effective on October 1, 2022.
This is the American ICD-10-CM version of E78.1 – other international versions of ICD-10 E78.1 may differ.