E78.3
BillableHyperchylomicronemia
Hyperchylomicronemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Chylomicron retention disease
- Fredrickson's hyperlipoproteinemia, type I or V
- Hyperlipidemia, group D
- Mixed hyperglyceridemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- sphingolipidosis (E75.0-E75.3)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hyperlipoproteinaemia3744001
- Hyperlipoproteinemia3744001
- Anapolipoproteinaemia33513003
- Anapolipoproteinemia33513003
- Familial apoC-II deficiency33513003
- Familial apolipoprotein C-II deficiency33513003
- Familial type 5 hyperlipoproteinaemia34349009
- Familial type 5 hyperlipoproteinemia34349009
- Familial type V hyperlipoproteinaemia34349009
- Familial type V hyperlipoproteinemia34349009
- Fredrickson type V hyperlipoproteinaemia34349009
- Fredrickson type V hyperlipoproteinemia34349009
- Familial hypertriglyceridaemia34528009
- Familial hypertriglyceridemia34528009
- Inborn error of lipoprotein metabolism43465001
- Familial lipoprotein deficiency49973006
- Familial hypobetalipoproteinaemia60193003
- Familial hypobetalipoproteinemia60193003
- Lipaemia retinalis95692001
- Lipemia retinalis95692001
- Lipidaemia retinalis95692001
- Lipidemia retinalis95692001
- Endogenous hyperlipaemia129589009
- Endogenous hyperlipemia129589009
- Endogenous hyperlipidaemia129589009
- Endogenous hyperlipidemia129589009
- Intestinal malabsorption197476001
- Intestinal malabsorption of fat197494007
- Primary hypertriglyceridaemia238083002
- Primary hypertriglyceridemia238083002
- Burger-Grutz syndrome267435002
- Familial hyperchylomicronaemia267435002
- Familial hyperchylomicronemia267435002
- Hyperchylomicronaemia267435002
- Hyperchylomicronemia267435002
- Primary hyperchylomicronaemia267435002
- Primary hyperchylomicronemia267435002
- Endogenous hypertriglyceridaemia275598004
- Endogenous hypertriglyceridemia275598004
- Familial fat-induced hypertriglyceridaemia275598004
- Familial fat-induced hypertriglyceridemia275598004
- Familial hyperlipoproteinaemia, type I275598004
- Familial hyperlipoproteinemia, type I275598004
- Familial lipoprotein lipase deficiency275598004
- Fredrickson type 1 hyperlipoproteinaemia275598004
- Fredrickson type 1 hyperlipoproteinemia275598004
- Hepatosplenomegalic lipoidosis275598004
- Hypercholesterinaemic xanthomatosis275598004
- Hypercholesterinemic xanthomatosis275598004
- Hyperlipoproteinaemia, type I275598004
- Hyperlipoproteinemia, type I275598004
- Primary acquired chylomicronemia402475008
- Xanthoma due to abnormality of lipid metabolism402724009
- Hyperlipidaemia with lipid deposition in skin402725005
- Hyperlipidemia with lipid deposition in skin402725005
- Primary chylomicronemia402726006
- Primary genetic hyperlipidaemia402785008
- Primary genetic hyperlipidemia402785008
- Chylomicronemia syndrome402786009
- Familial lipoprotein lipase deficiency with type I phenotype403827000
- Familial type I hyperlipoproteinaemia403827000
- Familial type I hyperlipoproteinemia403827000
- Familial lipoprotein lipase deficiency with type V phenotype403828005
- Anderson syndrome702364003
- Chylomicron retention disease702364003
- Lipid transport defect of intestine702364003
- Familial chylomicronemia syndrome1197489003
- Xanthoma due to primary chylomicronaemia1258977001
- Xanthoma due to primary chylomicronemia1258977001
UMLS
- ANDDC0795956
- ANDERSON DISEASEC0795956
- Anderson DiseaseC0795956
- Anderson SyndromeC0795956
- Anderson diseaseC0795956
- Anderson syndromeC0795956
- CHYLOMICRON RETENTION DISEASEC0795956
- CMRDC0795956
- CRDC0795956
- Chylomicron retention diseaseC0795956
- Chylomicron retention disease (disorder)C0795956
- HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKE PROTEIN IN INTESTINAL CELLSC0795956
- Hypobetalipoproteinemia with Accumulation of Apolipoprotein B-Like Protein In Intestinal CellsC0795956
- Hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cellsC0795956
- LIPID TRANSPORT DEFECT OF INTESTINEC0795956
- Lipid transport defect of intestineC0795956
- anderson diseaseC0795956
- anderson's diseaseC0795956
- andersons diseaseC0795956
- andersons syndromeC0795956
- disease andersonC0795956
- Burger Grutz SyndromeC0023817
- Burger Grutz syndromeC0023817
- Burger-Grutz SyndromeC0023817
- Burger-Grutz SyndromesC0023817
- Burger-Grutz syndromeC0023817
- CHYLOMICRONEMIA, FAMILIALC0023817
- Chylomicronemia, FamilialC0023817
- Chylomicronemias, FamilialC0023817
- Deficiencies, Familial LPLC0023817
- Deficiencies, LIPDC0023817
- Deficiencies, Lipase DC0023817
- Deficiencies, Lipoprotein LipaseC0023817
- Deficiency, Familial LPLC0023817
- Deficiency, LIPDC0023817
- Deficiency, Lipase DC0023817
- Deficiency, Lipoprotein LipaseC0023817
- Endogenous hypertriglyceridaemiaC0023817
- Endogenous hypertriglyceridemiaC0023817
- Essential Familial HyperlipemiaC0023817
- Essential Familial HyperlipemiasC0023817
- FAMILIAL LIPOPROTEIN LIPASE DEFICC0023817
- Familial ChylomicronemiaC0023817
- Familial Chylomicronemia SyndromC0023817
- Familial ChylomicronemiasC0023817
- Familial Essential HyperlipemiaC0023817
- Familial HyperchylomicronemiaC0023817
- Familial Hyperchylomicronemia SyndromeC0023817
- Familial HyperchylomicronemiasC0023817
- Familial Hyperlipemia, EssentialC0023817
- Familial Hyperlipemias, EssentialC0023817
- Familial Hyperlipoproteinemia Type 1C0023817
- Familial LPL DeficienciesC0023817
- Familial LPL DeficiencyC0023817
- Familial LPL deficiencyC0023817
- Familial Lipoprotein Lipase DeficiencyC0023817
- Familial fat-induced hypertriglyceridaemiaC0023817
- Familial fat-induced hypertriglyceridemiaC0023817
- Familial hyperchylomicronaemiaC0023817
- Familial hyperchylomicronemiaC0023817
- Familial hyperchylomicronemia (disorder)C0023817
- Familial hyperlipoproteinaemia, type IC0023817
- Familial hyperlipoproteinemia, type IC0023817
- Familial lipoprotein lipase deficiencyC0023817
- Familial lipoprotein lipase deficiency (disorder)C0023817
- Familial lipoprotein lipase deficiency with type I phenotypeC0023817
- Familial lipoprotein lipase deficiency with type I phenotype (disorder)C0023817
- Familial type I hyperlipoproteinaemiaC0023817
- Familial type I hyperlipoproteinemiaC0023817
- Fredrickson type 1 hyperlipoproteinaemiaC0023817
- Fredrickson type 1 hyperlipoproteinemiaC0023817
- Fredrickson's hyperlipoproteinemia, type I or VC0023817
- HYPERCHYLOMICRONEMIA, FAMILIALC0023817
- HYPERLIPEMIA, ESSENTIAL FAMILIALC0023817
- HYPERLIPEMIA, IDIOPATHIC, BURGER-GRUTZ TYPEC0023817
- HYPERLIPOPROTEINEMIA, TYPE IC0023817
- HYPERLIPOPROTEINEMIA, TYPE IAC0023817
- Hepatosplenomegalic lipoidosisC0023817
- Hypercholesterinaemic xanthomatosisC0023817
- Hypercholesterinemic xanthomatosisC0023817
- HyperchylomicronaemiaC0023817
- HyperchylomicronemiaC0023817
- Hyperchylomicronemia, FamilialC0023817
- Hyperchylomicronemias, FamilialC0023817
- Hyperlipemia, Essential FamilialC0023817
- Hyperlipemia, Idiopathic, Burger-Grutz TypeC0023817
- Hyperlipemias, Essential FamilialC0023817
- Hyperlipidemia, group DC0023817
- Hyperlipoproteinaemia, type IC0023817
- Hyperlipoproteinemia Type 1AC0023817
- Hyperlipoproteinemia Type IC0023817
- Hyperlipoproteinemia Type IaC0023817
- Hyperlipoproteinemia Type IasC0023817
- Hyperlipoproteinemia Type IsC0023817
- Hyperlipoproteinemia type IC0023817
- Hyperlipoproteinemia type IaC0023817
- Hyperlipoproteinemia, Type 1C0023817
- Hyperlipoproteinemia, Type IC0023817
- Hyperlipoproteinemia, Type IaC0023817
- Hyperlipoproteinemia, type IC0023817
- Hyperlipoproteinemias, Type IC0023817
- Hyperlipoproteinemias, Type IaC0023817
- LIPASE D DEFICIENCYC0023817
- LIPD DEFICIENCYC0023817
- LIPD DeficienciesC0023817
- LIPD DeficiencyC0023817
- LIPD deficiencyC0023817
- LIPOPROTEIN LIPASE DEFIC FAMILIALC0023817
- LIPOPROTEIN LIPASE DEFICIENCYC0023817
- LPL DEFICIENCYC0023817
- LPL Deficiencies, FamilialC0023817
- LPL Deficiency, FamilialC0023817
- Lipase D DeficienciesC0023817
- Lipase D DeficiencyC0023817
- Lipase D deficiencyC0023817
- Lipase Deficiencies, LipoproteinC0023817
- Lipoprotein Lipase DeficienciesC0023817
- Lipoprotein Lipase DeficiencyC0023817
- Lipoprotein Lipase Deficiency, FamilialC0023817
- Lipoprotein lipase deficiency, familialC0023817
- Lipoprotein-lipase deficiencyC0023817
- Mixed hyperglyceridemiaC0023817
- Primary hyperchylomicronaemiaC0023817
- Primary hyperchylomicronemiaC0023817
- Syndrome, Burger-GrutzC0023817
- Syndromes, Burger-GrutzC0023817
- Type I HyperlipoproteinemiaC0023817
- Type I HyperlipoproteinemiasC0023817
- Type I hyperlipoproteinaemiaC0023817
- Type I hyperlipoproteinemiaC0023817
- Type Ia HyperlipoproteinemiaC0023817
- Type Ia HyperlipoproteinemiasC0023817
- burger-grutz syndromeC0023817
- endogenous hypertriglyceridemiaC0023817
- familial hyperchylomicronemiaC0023817
- familial hyperlipoproteinemia type IC0023817
- familial lipoprotein lipase deficiencyC0023817
- hyperchylomicronemiaC0023817
- hyperlipoproteinemia type iC0023817
- type i hyperlipoproteinemiaC0023817
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.
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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.