E78.2
BillableMixed hyperlipidemia
Mixed hyperlipidemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Broad- or floating-betalipoproteinemia
- Combined hyperlipidemia NOS
- Elevated cholesterol with elevated triglycerides NEC
- Fredrickson's hyperlipoproteinemia, type IIb or III
- Hyperbetalipoproteinemia with prebetalipoproteinemia
- Hypercholesteremia with endogenous hyperglyceridemia
- Hyperlipidemia, group C
- Tubo-eruptive xanthoma
- Xanthoma tuberosum
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)
- cerebrotendinous cholesterosis [van Bogaert-Scherer- Epstein] (E75.5)
- familial combined hyperlipidemia (E78.49)
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
- Xanthoma63103006
- Xanthomatosis63103006
- Endogenous hyperlipaemia129589009
- Endogenous hyperlipemia129589009
- Endogenous hyperlipidaemia129589009
- Endogenous hyperlipidemia129589009
- Mixed hypercholesterolaemia and hypertriglyceridaemia129591001
- Mixed hypercholesterolemia and hypertriglyceridemia129591001
- Diabetic xanthoma217341008
- Xanthoma diabeticorum217341008
- Xanthomatosis, familial238074007
- Primary combined hyperlipidaemia238088006
- Primary combined hyperlipidemia238088006
- Primary mixed hyperlipidaemia238088006
- Primary mixed hyperlipidemia238088006
- Secondary combined hyperlipidaemia238089003
- Secondary combined hyperlipidemia238089003
- Secondary mixed hyperlipidaemia238089003
- Secondary mixed hyperlipidemia238089003
- Eruptive xanthoma238952003
- Plane xanthoma238953008
- Tuberous xanthoma238954002
- Xanthoma tuberosum238954002
- Generalised plane xanthoma238955001
- Generalized plane xanthoma238955001
- Mixed hyperlipidaemia267434003
- Mixed hyperlipidemia267434003
- Multiple-type hyperlipidaemia267434003
- Multiple-type hyperlipidemia267434003
- Apolipoprotein E deficiency398796005
- Broad beta disease398796005
- Carbohydrate induced hyperlipaemia398796005
- Carbohydrate induced hyperlipemia398796005
- Dysbetalipoproteinaemia398796005
- Dysbetalipoproteinemia398796005
- Familial dysbetalipoproteinaemia398796005
- Familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia398796005
- Familial hyperbetalipoproteinemia and hyperprebetalipoproteinemia398796005
- Familial hypercholesterolaemia with hyperlipaemia398796005
- Familial hypercholesterolemia with hyperlipemia398796005
- Familial type 3 hyperlipoproteinaemia398796005
- Familial type 3 hyperlipoproteinemia398796005
- Familial type III hyperlipoproteinaemia398796005
- Floating beta disease398796005
- Fredrickson type III hyperlipoproteinaemia398796005
- Fredrickson type III hyperlipoproteinemia398796005
- Primary dysbetalipoproteinaemia398796005
- Primary dysbetalipoproteinemia398796005
- Remnant hyperlipidaemia398796005
- Remnant hyperlipidemia398796005
- Remnant hyperlipoproteinaemia398796005
- Remnant hyperlipoproteinemia398796005
- Diffuse xanthoma399970005
- Disseminated xanthosiderohistiocytosis399970005
- Xanthoma disseminatum399970005
- Tubero-eruptive xanthoma402471004
- Cutaneous xanthoma402472006
- Primary polygenic type IIb combined hyperlipidaemia402474007
- Primary polygenic type IIb combined hyperlipidemia402474007
- Xanthoma due to lymphedema402476009
- Xanthoma due to lymphoedema402476009
- Secondary xanthomatous infiltration of the skin402478005
- Xanthoma due to abnormality of lipid metabolism402724009
- Primary genetic hyperlipidaemia402785008
- Primary genetic hyperlipidemia402785008
- Primary genetic mixed hyperlipidaemia402787000
- Primary genetic mixed hyperlipidemia402787000
- Atypical xanthoma disseminatum404163009
- Diffuse normolipemic plane xanthomatosis404163009
- Diffuse plane xanthomatosis404163009
- Diffuse plane xanthoma due to hyperlipidaemia1251362006
- Diffuse plane xanthoma due to hyperlipidemia1251362006
- Palmar xanthoma1254896008
- Xanthomatosis of skin of palm1254896008
- Xanthomatosis of skin of palm of hand1254896008
- Xanthoma due to primary combined hyperlipidaemia1256073006
- Xanthoma due to primary combined hyperlipidemia1256073006
- Mixed hyperlipidaemia due to type 1 diabetes mellitus1571000119104
- Mixed hyperlipidemia due to type 1 diabetes mellitus1571000119104
- Mixed hyperlipidaemia due to type 2 diabetes mellitus701000119103
- Mixed hyperlipidaemia due to type II diabetes mellitus701000119103
- Mixed hyperlipidemia due to type 2 diabetes mellitus701000119103
- Mixed hyperlipidemia due to type II diabetes mellitus701000119103
UMLS
- APOLIPOPROTEIN B-100, FAMILIAL DEFECTIVEC1704417
- APOLIPOPROTEIN B-100, FAMILIAL LIGAND-DEFECTIVEC1704417
- Apolipoprotein B 100, Familial DefectiveC1704417
- Apolipoprotein B 100, Familial Ligand DefectiveC1704417
- Apolipoprotein B-100, Familial DefectiveC1704417
- Apolipoprotein B-100, Familial Ligand-DefectiveC1704417
- Autosomal Dominant HypercholesterolemiaC1704417
- Combined Hyperlipoproteinemia, FamilialC1704417
- Combined Hyperlipoproteinemias, FamilialC1704417
- FCHL - Familial combined hyperlipidaemiaC1704417
- FCHL - Familial combined hyperlipidemiaC1704417
- FCHL2C1704417
- FDB - Familial defective apolipoprotein B-100C1704417
- FHCL2C1704417
- Familial Combined HyperlipoproteinemiaC1704417
- Familial Combined HyperlipoproteinemiasC1704417
- Familial Hypercholesterolemia 2C1704417
- Familial defective apolipoprotein B-100C1704417
- Familial defective apolipoprotein B-100 (disorder)C1704417
- Familial hyperlipoproteinaemia type IIbC1704417
- Familial hyperlipoproteinemia type IIbC1704417
- Fredrickson Type IIb hyperlipoproteinaemiaC1704417
- Fredrickson Type IIb hyperlipoproteinemiaC1704417
- Fredrickson type IIb hyperlipoproteinaemiaC1704417
- Fredrickson type IIb hyperlipoproteinemiaC1704417
- Fredrickson's hyperlipoproteinemia, type IIb or IIIC1704417
- HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE BC1704417
- HYPERCHOLESTEROLEMIA, FAMILIAL, 2C1704417
- HyperapobetalipoproteinaemiaC1704417
- HyperapobetalipoproteinemiaC1704417
- Hyperbetalipoproteinemia with prebetalipoproteinemiaC1704417
- Hypercholesterolemia, Autosomal Dominant, Type BC1704417
- Hypercholesterolemia, Familial, 2C1704417
- Hyperlipoproteinemia Type IIbC1704417
- Hyperlipoproteinemia Type IIbsC1704417
- Hyperlipoproteinemia, Familial CombinedC1704417
- Hyperlipoproteinemias, Familial CombinedC1704417
- Type IIb hyperlipoproteinaemiaC1704417
- Type IIb hyperlipoproteinemiaC1704417
- Broad- or floating-betalipoproteinemiaC2047520
- Mixed hyperlipidaemiaC2047520
- Mixed hyperlipidemiaC2047520
- Mixed hyperlipidemia (disorder)C2047520
- Multiple-type hyperlipidaemiaC2047520
- Multiple-type hyperlipidemiaC2047520
- Combined hyperlipidaemiaC2712907
- Combined hyperlipidemiaC2712907
- Combined hyperlipidemia NOSC2712907
- combined hyperlipidemiaC2712907
- Elevated cholesterol with elevated triglycerides NECC2712905
- Hypercholesteremia with endogenous hyperglyceridemiaC2874289
- Hyperlipidemia, group CC1399990
- Tuberous xanthomaC0302164
- Tuberous xanthoma (disorder)C0302164
- Tubo-eruptive xanthomaC0302164
- Xanthoma tuberosumC0302164
- tuberous xanthomaC0302164
- tuberous xanthomasC0302164
- xanthoma tuberosumC0302164
Frequently Asked Questions
What is the ICD-10 code for mixed hyperlipidemia?
The ICD-10-CM code for mixed hyperlipidemia is E78.2. The full clinical description is "Mixed hyperlipidemia". E78.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E78.2 mean?
ICD-10-CM code E78.2 represents "Mixed hyperlipidemia". 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 E78.2 a billable code?
Yes, E78.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.2 in?
E78.2 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.2?
E78.2 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 6 more.
What SNOMED CT codes does E78.2 map to?
E78.2 maps to 29 SNOMED CT concepts: 398796005, 404163009, 402472006, 217341008, 1251362006, and 24 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.2?
E78.2 is linked to 7 UMLS Concept Unique Identifiers: C1704417, C2047520, C2712907, C2712905, C2874289, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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.
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.