E78.49
BillableOther hyperlipidemia
Other hyperlipidemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Familial combined hyperlipidemia
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
- Exogenous hyperlipaemia129590000
- Exogenous hyperlipemia129590000
- Exogenous hyperlipidaemia129590000
- Exogenous hyperlipidemia129590000
- FCHL - Familial combined hyperlipidaemia238040008
- FCHL - Familial combined hyperlipidemia238040008
- Familial combined hyperlipidaemia238040008
- Familial combined hyperlipidemia238040008
- Familial hyperlipoproteinaemia type IIb238040008
- Familial hyperlipoproteinemia type IIb238040008
- Fredrickson type IIb hyperlipoproteinaemia238040008
- Fredrickson type IIb hyperlipoproteinemia238040008
- Hyperapobetalipoproteinaemia238040008
- Hyperapobetalipoproteinemia238040008
- Secondary hypercholesterolaemia238082007
- Secondary hypercholesterolemia238082007
- Primary combined hyperlipidaemia238088006
- Primary combined hyperlipidemia238088006
- Primary mixed hyperlipidaemia238088006
- Primary mixed hyperlipidemia238088006
- Mixed hyperlipidaemia267434003
- Mixed hyperlipidemia267434003
- Multiple-type hyperlipidaemia267434003
- Multiple-type hyperlipidemia267434003
- Familial multiple lipoprotein-type hyperlipidaemia299465007
- Familial multiple lipoprotein-type hyperlipidemia299465007
- Secondary hyperlipidaemia402727002
- Secondary hyperlipidemia402727002
- Chemically induced hyperlipidaemia426161002
- Chemically induced hyperlipidemia426161002
UMLS
- Combined Hyperlipidemia, FamilialC0020474
- Combined Hyperlipidemias, FamilialC0020474
- FAMILIAL COMBINED HYPERLIPIDEMIAC0020474
- FCHL3C0020474
- Familial Combined HyperlipidemiaC0020474
- Familial Combined HyperlipidemiasC0020474
- Familial combined hyperlipidaemiaC0020474
- Familial combined hyperlipidemiaC0020474
- Familial combined hyperlipidemia (disorder)C0020474
- Familial multiple lipoprotein-type hyperlipidaemiaC0020474
- Familial multiple lipoprotein-type hyperlipidemiaC0020474
- Familial multiple lipoprotein-type hyperlipidemia (disorder)C0020474
- HYPERLIPIDEMIA, FAMILIAL COMBINED, 3C0020474
- HyperapobetalipoproteinemiaC0020474
- Hyperlipidemia Type IIbC0020474
- Hyperlipidemia, Familial CombinedC0020474
- Hyperlipidemia, Multiple Lipoprotein TypeC0020474
- Hyperlipidemia, Multiple Lipoprotein-TypeC0020474
- Hyperlipidemias, Familial CombinedC0020474
- Hyperlipidemias, Multiple Lipoprotein-TypeC0020474
- Hyperlipoproteinemia, Type IIbC0020474
- Lipoprotein-Type Hyperlipidemia, MultipleC0020474
- Lipoprotein-Type Hyperlipidemias, MultipleC0020474
- Multiple Lipoprotein-Type HyperlipidemiaC0020474
- Multiple Lipoprotein-Type HyperlipidemiasC0020474
- Type IIb HyperlipidemiaC0020474
- Type IIb HyperlipoproteinemiaC0020474
- Type IIb hyperlipidaemiaC0020474
- Type IIb hyperlipidemiaC0020474
- broad floating betalipoproteinemiaC0020474
- disorder hyperlipidemia mixedC0020474
- familial combined hyperlipidemiaC0020474
- mixed hyperlipidemiaC0020474
- Other hyperlipidemiaC0348494
Frequently Asked Questions
What is the ICD-10 code for other hyperlipidemia?
The ICD-10-CM code for other hyperlipidemia is E78.49. The full clinical description is "Other hyperlipidemia". E78.49 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E78.49 mean?
ICD-10-CM code E78.49 represents "Other 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 E78.49 a billable code?
Yes, E78.49 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.49 in?
E78.49 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.49?
E78.49 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 E78.49 map to?
E78.49 maps to 8 SNOMED CT concepts: 426161002, 129590000, 238040008, 299465007, 267434003, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.49?
E78.49 is linked to 2 UMLS Concept Unique Identifiers: C0020474, C0348494. 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.