Lipaemia retinalis
burger-grutz syndrome
Familial Chylomicronemia Syndrom
Hyperlipoproteinemia type I
Familial type V hyperlipoproteinaemia
Lipoprotein Lipase Deficiency
Fredrickson type V hyperlipoproteinemia
Hyperlipoproteinemia, type I
Primary genetic hyperlipidemia
Primary chylomicronemia
Type I Hyperlipoproteinemias
FAMILIAL LIPOPROTEIN LIPASE DEFIC
Lipemia retinalis
Chylomicronemia syndrome
Familial lipoprotein lipase deficiency
Xanthoma due to primary chylomicronaemia
Hyperlipoproteinemia type Ia
type i hyperlipoproteinemia
Familial Essential Hyperlipemia
Familial type I hyperlipoproteinemia
anderson disease
Familial chylomicronemia syndrome
LIPD Deficiency
Familial hypobetalipoproteinemia
Familial hyperlipoproteinemia, type I
CMRD
LIPD Deficiencies
disease anderson
Type Ia Hyperlipoproteinemias
Deficiencies, Familial LPL
Familial Chylomicronemias
CHYLOMICRONEMIA, FAMILIAL
Deficiencies, LIPD
Burger Grutz syndrome
CRD
Hyperlipoproteinemias, Type Ia
Chylomicron retention disease
Familial type 5 hyperlipoproteinemia
Familial Hyperchylomicronemias
Lipase Deficiencies, Lipoprotein
Hyperlipemias, Essential Familial
Deficiencies, Lipase D
LPL Deficiencies, Familial
Hypercholesterinaemic xanthomatosis
Hyperlipidemia with lipid deposition in skin
Xanthoma due to primary chylomicronemia
Essential Familial Hyperlipemia
LIPOPROTEIN LIPASE DEFIC FAMILIAL
Familial hypertriglyceridemia
Xanthoma due to abnormality of lipid metabolism
Familial hyperchylomicronemia
Familial apoC-II deficiency
Intestinal malabsorption of fat
Endogenous hyperlipidaemia
Lipidaemia retinalis
Hyperlipoproteinaemia
LIPASE D DEFICIENCY
Familial type V hyperlipoproteinemia
Chylomicronemias, Familial
Hyperlipoproteinemia Type 1A
Endogenous hyperlipidemia
Familial hyperchylomicronaemia
Familial hypobetalipoproteinaemia
Deficiency, LIPD
Inborn error of lipoprotein metabolism
Hypercholesterinemic xanthomatosis
Primary hyperchylomicronaemia
Primary acquired chylomicronemia
Familial Hyperlipemias, Essential
Familial lipoprotein lipase deficiency (disorder)
Familial Hyperlipoproteinemia Type 1
Anapolipoproteinaemia
Hyperlipoproteinemia
Primary hypertriglyceridemia
Syndrome, Burger-Grutz
Hyperlipoproteinemia, Type Ia
LPL Deficiency, Familial
Hyperchylomicronemias, Familial
Lipidemia retinalis
LPL DEFICIENCY
Anderson Syndrome
Hyperlipidaemia with lipid deposition in skin
Endogenous hypertriglyceridaemia
Hyperchylomicronemia, Familial
andersons disease
familial hyperlipoproteinemia type I
anderson's disease
Familial hyperlipoproteinaemia, type I
Familial Hyperlipemia, Essential
Lipoprotein Lipase Deficiencies
Deficiency, Lipase D
Burger-Grutz Syndromes
Deficiency, Lipoprotein Lipase
Familial Chylomicronemia
Familial fat-induced hypertriglyceridaemia
Familial lipoprotein lipase deficiency with type V phenotype
Hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells
Primary genetic hyperlipidaemia
andersons syndrome
Familial LPL Deficiencies
Lipase D Deficiencies
Endogenous hyperlipemia
HYPERLIPEMIA, ESSENTIAL FAMILIAL
Hyperlipemia, Idiopathic, Burger-Grutz Type
Hyperchylomicronaemia
Essential Familial Hyperlipemias
Hyperlipoproteinemia Type Is
Mixed hyperglyceridemia
Familial type 5 hyperlipoproteinaemia
Familial lipoprotein lipase deficiency with type I phenotype
Deficiencies, Lipoprotein Lipase
Familial Hyperchylomicronemia Syndrome
Lipoprotein-lipase deficiency
Chylomicron retention disease (disorder)
Type Ia Hyperlipoproteinemia
Familial hypertriglyceridaemia
Primary hypertriglyceridaemia
Familial LPL deficiency
Hyperlipoproteinaemia, type I
Hyperlipoproteinemia Type Ias
Hyperlipidemia, group D
Type I hyperlipoproteinaemia
Hepatosplenomegalic lipoidosis
Endogenous hyperlipaemia
ANDD
Familial lipoprotein deficiency
endogenous hypertriglyceridemia
Primary hyperchylomicronemia
Familial fat-induced hypertriglyceridemia
Hyperlipoproteinemias, Type I
Fredrickson type V hyperlipoproteinaemia
Fredrickson's hyperlipoproteinemia, type I or V
Deficiency, Familial LPL
Familial lipoprotein lipase deficiency with type I phenotype (disorder)
Fredrickson type 1 hyperlipoproteinemia
Familial apolipoprotein C-II deficiency
Intestinal malabsorption
Lipoprotein Lipase Deficiency, Familial
LIPID TRANSPORT DEFECT OF INTESTINE
Anapolipoproteinemia
Fredrickson type 1 hyperlipoproteinaemia
Familial hyperchylomicronemia (disorder)
Syndromes, Burger-Grutz
Hyperlipoproteinemia, Type 1
Familial type I hyperlipoproteinaemia

Frequently Asked Questions

What is the ICD-10 code for hyperchylomicronemia?

The ICD-10-CM code for hyperchylomicronemia is E78.3. The full clinical description is "Hyperchylomicronemia". E78.3 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E78.3 mean?

ICD-10-CM code E78.3 represents “Hyperchylomicronemia”. 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 E78.3 a billable code?

Yes, E78.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E78.3 in?

E78.3 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E78.3?

E78.3 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 E78.3 map to?

E78.3 maps to 25 SNOMED CT concepts: 33513003, 702364003, 267435002, 402786009, 129589009, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E78.3?

E78.3 is linked to 2 UMLS Concept Unique Identifiers: C0795956, C0023817. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E78.3 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hyperchylomicronemia 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 E78.3?

E78.3 maps to the ICD-11 code: 5C80.1 (Hypertriglyceridaemia).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try Free View API Docs

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.