- E78.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM E78.3 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E78.3 – other international versions of ICD-10 E78.3 may differ.
ICD-10-CM E78.3 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Chylomicron retention disease
- Fredrickson’s hyperlipoproteinemia, type I or V
- Hyperlipidemia, group D
- Mixed hyperglyceridemia
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to E78.3:
- Bürger-Grütz (essential familial hyperlipemia) > Disease, diseased
- chylomicron retention > Disease, diseased
- I and V > Frederickson\’s hyperlipoproteinemia, type
- hyperlipemic (Bürger-Grütz type) > Hepatosplenomegaly R16.2
- with hyperbetalipoproteinemia > Hyperchylomicronemia (familial) (primary) E78.3
- mixed > Hyperglyceridemia (endogenous) (essential) (familial) (hereditary) (pure) E78.1
- D > group E78.00
- Fredrickson\’s type > Hyperlipoproteinemia E78.5
- I > Fredrickson\’s type E78.3
- V > Fredrickson\’s type E78.3
- retina, retinalis > Lipemia
- hepatosplenomegalic > Lipidosis E75.6
- with chylomicronemia > Prebetalipoproteinemia (acquired) (essential) (familial) (hereditary) (primary) (secondary) E78.1
- Bürger-Grütz > Syndrome
- hyperlipoproteinemia > with
- Type I > hyperlipoproteinemia E78.3
- Type V > hyperlipoproteinemia E78.3