E78.1
BillablePure hyperglyceridemia
Pure hyperglyceridemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Elevated fasting triglycerides
- Endogenous hyperglyceridemia
- Fredrickson's hyperlipoproteinemia, type IV
- Hyperlipidemia, group B
- Hyperprebetalipoproteinemia
- Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(9)
E78.0Pure hypercholesterolemia
E78.2Mixed hyperlipidemia
E78.3Hyperchylomicronemia
E78.4Other hyperlipidemia
E78.5Hyperlipidemia, unspecified
E78.6Lipoprotein deficiency
E78.7Disorders of bile acid and cholesterol metabolism
E78.8Other disorders of lipoprotein metabolism
E78.9Disorder of lipoprotein metabolism, unspecified
Related Conditions
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(166)
SNOMED CT
- Hyperlipoproteinaemia3744001
- Hyperlipoproteinemia3744001
- Familial hypertriglyceridaemia34528009
- Familial hypertriglyceridemia34528009
- Endogenous hyperlipaemia129589009
- Endogenous hyperlipemia129589009
- Endogenous hyperlipidaemia129589009
- Endogenous hyperlipidemia129589009
- Primary hypertriglyceridaemia238083002
- Primary hypertriglyceridemia238083002
- Very low density lipoprotinaemia238084008
- Very low density lipoprotinemia238084008
- Fredrickson type IV hyperlipoproteinaemia238085009
- Fredrickson type IV hyperlipoproteinemia238085009
- Fredrickson type IV lipidaemia238085009
- Fredrickson type IV lipidemia238085009
- Secondary hypertriglyceridaemia238087001
- Secondary hypertriglyceridemia238087001
- Pure hyperglyceridaemia267433009
- Pure hyperglyceridemia267433009
- Hypertriglyceridaemia302870006
- Hypertriglyceridemia302870006
- Sporadic primary hypertriglyceridaemia402473001
- Sporadic primary hypertriglyceridemia402473001
- Xanthoma due to abnormality of lipid metabolism402724009
- Primary genetic hyperlipidaemia402785008
- Primary genetic hyperlipidemia402785008
- Transient infantile hypertriglyceridaemia and fatty liver773649005
- Transient infantile hypertriglyceridaemia and hepatosteatosis773649005
- Transient infantile hypertriglyceridemia and fatty liver773649005
- Transient infantile hypertriglyceridemia and hepatosteatosis773649005
- Xanthoma due to primary hypertriglyceridaemia1256071008
- Xanthoma due to primary hypertriglyceridemia1256071008
UMLS
- CARBOHYDRATE-INDUCIBLE HYPERLIPEMIAC0020480
- Carbohydrate Inducible HyperlipemiaC0020480
- Carbohydrate Inducible HyperlipemiasC0020480
- Carbohydrate-Inducible HyperlipemiaC0020480
- Carbohydrate-Inducible HyperlipemiasC0020480
- Endogenous hyperglyceridemiaC0020480
- Endogenous hyperlipaemiaC0020480
- Endogenous hyperlipemiaC0020480
- Endogenous hyperlipidaemiaC0020480
- Endogenous hyperlipidemiaC0020480
- Endogenous hyperlipidemia (disorder)C0020480
- Familial Hyperlipoproteinemia Type 4C0020480
- Familial HypertriglyceridemiaC0020480
- Familial Type IV HyperlipoproteinemiaC0020480
- Familial hypertriglyceridaemiaC0020480
- Familial hypertriglyceridemiaC0020480
- Familial hypertriglyceridemia (disorder)C0020480
- Fredrickson Type IV LipidemiaC0020480
- Fredrickson Type IV lipidaemiaC0020480
- Fredrickson Type IV lipidemiaC0020480
- Fredrickson type IV hyperlipoproteinaemiaC0020480
- Fredrickson type IV hyperlipoproteinemiaC0020480
- Fredrickson type IV hyperlipoproteinemia (disorder)C0020480
- Fredrickson type IV lipidaemiaC0020480
- Fredrickson type IV lipidemiaC0020480
- Fredrickson's hyperlipoproteinemia, type IVC0020480
- HYPERLIPOPROTEINEMIA, TYPE IVC0020480
- Hyper prebeta lipoproteinemiaC0020480
- Hyperlipemia, Carbohydrate InducibleC0020480
- Hyperlipemia, Carbohydrate-InducibleC0020480
- Hyperlipemias, Carbohydrate InducibleC0020480
- Hyperlipemias, Carbohydrate-InducibleC0020480
- Hyperlipidemia, group BC0020480
- Hyperlipoproteinemia Type IVC0020480
- Hyperlipoproteinemia, Type IVC0020480
- Hyperlipoproteinemias, Type IVC0020480
- HyperprebetalipoproteinemiaC0020480
- Hypertriglyceridemia, FamilialC0020480
- Inducible Hyperlipemia, CarbohydrateC0020480
- Inducible Hyperlipemias, CarbohydrateC0020480
- Pure hyperglyceridaemiaC0020480
- Pure hyperglyceridemiaC0020480
- Pure hyperglyceridemia (disorder)C0020480
- Type IV HyperlipoproteinemiaC0020480
- Type IV HyperlipoproteinemiasC0020480
- Type IV hyperlipidaemiaC0020480
- Type IV hyperlipidemiaC0020480
- Type IV hyperlipoproteinaemiaC0020480
- Type IV hyperlipoproteinemiaC0020480
- Type IV lipidaemiaC0020480
- Type IV lipidemiaC0020480
- Type IV, HyperlipoproteinemiaC0020480
- Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinemiaC0020480
- endogenous hyperglyceridemiaC0020480
- endogenous hyperlipidemiaC0020480
- familial hyperlipoproteinemia type IVC0020480
- familial hyperprebetalipoproteinemiaC0020480
- familial hypertriglyceridaemiaC0020480
- familial hypertriglyceridemiaC0020480
- hyperlipidemia type ivC0020480
- type iv hyperlipidemiaC0020480
- type iv hyperlipoproteinemiaC0020480
- Elevated fasting triglyceridesC2874288
Clinical Terms
- Hyperlipoproteinemia Type IV
- HYPERLIPOPROTEINEMIA, TYPE IV
- Fredrickson Type IV Lipidemia
- familial hyperlipoproteinemia type IV
- Primary genetic hyperlipidemia
- Elevated fasting triglycerides
- Sporadic primary hypertriglyceridaemia
- Type IV hyperlipidemia
- Hyperlipemias, Carbohydrate-Inducible
- Hyperlipidemia, group B
- Hypertriglyceridaemia
- Very low density lipoprotinaemia
- Secondary hypertriglyceridemia
- hyperlipidemia type iv
- Hypertriglyceridemia
- Fredrickson's hyperlipoproteinemia, type IV
- Type IV Hyperlipoproteinemia
- Hypertriglyceridemia, Familial
- familial hyperprebetalipoproteinemia
- Familial Type IV Hyperlipoproteinemia
- Inducible Hyperlipemia, Carbohydrate
- Hyperlipoproteinemias, Type IV
- Familial hypertriglyceridemia
- Xanthoma due to abnormality of lipid metabolism
- Fredrickson type IV lipidaemia
- Endogenous hyperlipidaemia
- Hyperlipoproteinaemia
- Endogenous hyperlipidemia
- Xanthoma due to primary hypertriglyceridemia
- Type IV lipidaemia
- Transient infantile hypertriglyceridaemia and hepatosteatosis
- Hyperlipoproteinemia
- Primary hypertriglyceridemia
- Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinemia
- Endogenous hyperglyceridemia
- Hyper prebeta lipoproteinemia
- Type IV Hyperlipoproteinemias
- Carbohydrate Inducible Hyperlipemias
- Type IV hyperlipoproteinaemia
- Transient infantile hypertriglyceridaemia and fatty liver
- Inducible Hyperlipemias, Carbohydrate
- Sporadic primary hypertriglyceridemia
- Carbohydrate-Inducible Hyperlipemia
- Familial Hyperlipoproteinemia Type 4
- Transient infantile hypertriglyceridemia and hepatosteatosis
- Primary genetic hyperlipidaemia
- Hyperlipemia, Carbohydrate-Inducible
- Type IV, Hyperlipoproteinemia
- Endogenous hyperlipemia
- Pure hyperglyceridaemia
- Transient infantile hypertriglyceridemia and fatty liver
- Familial hypertriglyceridemia (disorder)
- Very low density lipoprotinemia
- Carbohydrate Inducible Hyperlipemia
- Familial hypertriglyceridaemia
- Primary hypertriglyceridaemia
- Endogenous hyperlipidemia (disorder)
- Pure hyperglyceridemia (disorder)
- Fredrickson type IV hyperlipoproteinaemia
- Hyperlipemias, Carbohydrate Inducible
- Carbohydrate-Inducible Hyperlipemias
- Endogenous hyperlipaemia
- Type IV lipidemia
- Xanthoma due to primary hypertriglyceridaemia
- Secondary hypertriglyceridaemia
- Fredrickson type IV hyperlipoproteinemia
- Type IV hyperlipidaemia
- Hyperprebetalipoproteinemia
- Hyperlipemia, Carbohydrate Inducible
- Fredrickson type IV hyperlipoproteinemia (disorder)
Frequently Asked Questions
What is the ICD-10 code for pure hyperglyceridemia?
The ICD-10-CM code for pure hyperglyceridemia is E78.1. The full clinical description is "Pure hyperglyceridemia". E78.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E78.1 mean?
ICD-10-CM code E78.1 represents “Pure hyperglyceridemia”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E78.1 a billable code?
Yes, E78.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.1 in?
E78.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.1?
E78.1 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 4 more.
What SNOMED CT codes does E78.1 map to?
E78.1 maps to 14 SNOMED CT concepts: 129589009, 34528009, 238085009, 3744001, 302870006, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.1?
E78.1 is linked to 2 UMLS Concept Unique Identifiers: C0020480, C2874288. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E78.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like pure hyperglyceridemia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E78.1?
E78.1 maps to the ICD-11 code: 5C80.1 (Hypertriglyceridaemia).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.