Category · FY2027
E78 Disorders of lipoprotein metabolism and other lipidemias
- Header · not billable
E78 is not billable. The category heads 18 billable codes in FY2027, grouped under 10 subdivisions.
ICD-10 code by name
- What is the ICD-10 code for hyperlipidemia, unspecified?
- Hyperlipidemia ICD-10 code: E78.5 Hyperlipidemia, unspecified. Search ICD-10 for hyperlipidemia
- What is the ICD-10 code for mixed hyperlipidemia?
- Mixed hyperlipidemia ICD-10 code: E78.2 Mixed hyperlipidemia. Search ICD-10 for mixed hyperlipidemia
- What is the ICD-10 code for other hyperlipidemia?
- Other hyperlipidemia ICD-10 code: E78.49 Other hyperlipidemia. Search ICD-10 for other hyperlipidemia
Where it sits
- Chapter 4 Endocrine, nutritional and metabolic diseases (E00-E89)
- E70-E88 Metabolic disorders (E70-E88)
- E78 Disorders of lipoprotein metabolism and other lipidemias
- Billable codes
- 18
- Subdivisions
- 10
- CC / MCC codes
- 2 / 0
- HCC V28 codes
- 0
- New FY2027
- 0
- Index entries
- 95
Codes in E78
- E78.0Pure hypercholesterolemiaHeader
- E78.00Pure hypercholesterolemia, unspecifiedBillable
Inclusion terms 4
Inclusion terms
- Fredrickson's hyperlipoproteinemia, type IIa
- Hyperbetalipoproteinemia
- Low-density-lipoprotein-type [LDL] hyperlipoproteinemia
- (Pure) hypercholesterolemia NOS
- E78.01Familial hypercholesterolemiaHeader
- E78.010Homozygous familial hypercholesterolemia [HoFH]Billable
- E78.011Heterozygous familial hypercholesterolemia [HeFH]Billable
- E78.019Familial hypercholesterolemia, unspecifiedBillable
Inclusion terms 1
Inclusion terms
- Familial hypercholesterolemia NOS
- E78.1Pure hyperglyceridemia 1 billable codeBillable
- E78.2Mixed hyperlipidemia 1 billable codeBillable
- E78.3HyperchylomicronemiaBillable
Inclusion terms 4
Inclusion terms
- Chylomicron retention disease
- Fredrickson's hyperlipoproteinemia, type I or V
- Hyperlipidemia, group D
- Mixed hyperglyceridemia
- E78.4Other hyperlipidemiaHeader
- E78.41Elevated Lipoprotein(a)Billable
Inclusion terms 1
Inclusion terms
- Elevated Lp(a)
- E78.49Other hyperlipidemia 1 billable codeBillable
- E78.5Hyperlipidemia, unspecified 1 billable codeBillable
- E78.6Lipoprotein deficiencyBillable
Inclusion terms 7
Inclusion terms
- Abetalipoproteinemia
- Depressed HDL cholesterol
- High-density lipoprotein deficiency
- Hypoalphalipoproteinemia
- Hypobetalipoproteinemia (familial)
- Lecithin cholesterol acyltransferase deficiency
- Tangier disease
- E78.7Disorders of bile acid and cholesterol metabolismHeader
Excludes1 1
Excludes1
- Niemann-Pick disease type C (E75.242) E75.242
- E78.70Disorder of bile acid and cholesterol metabolism, unspecifiedBillable
- E78.71Barth syndromeBillableCC
- E78.72Smith-Lemli-Opitz syndromeBillableCC
- E78.79Other disorders of bile acid and cholesterol metabolismBillable
- E78.8Other disorders of lipoprotein metabolismHeader
- E78.81Lipoid dermatoarthritisBillable
- E78.89Other lipoprotein metabolism disordersBillable
- E78.9Disorder of lipoprotein metabolism, unspecifiedBillable
CC/MCC: as a secondary diagnosis, unless the principal diagnosis is on the code’s PDX exclusion list (MS-DRG v44 Appendix C; list on the code card).
Instructions
Notes that also apply
Block E70-E88 instructions (Excludes1 5, Excludes2 1): printed on the block page.
Chapter 4 instructions (Notes 1, Excludes1 1): printed on the chapter 4 page.
Index entries
- Cholesteremia → E78.00
- Cholesterolemia (essential) (pure) → E78.00
- Hyperbetalipoproteinemia (familial) → E78.00
- Hypercholesterolemia (essential) (primary) (pure) → E78.00
- Low-density-lipoprotein-type (LDL) hyperlipoproteinemia → E78.00
- HoFH (homozygous familial hypercholesterolemia) → E78.010
- HeFH (heterozygous familial hypercholesterolemia) → E78.011
- Bürger-Grütz disease or syndrome → E78.3
- Chylomicronemia (fasting) (with hyperprebetalipoproteinemia) → E78.3
- Hyperchylomicronemia (familial) (primary) → E78.3
- Abetalipoproteinemia → E78.6
- Acanthocytosis → E78.6
- Analphalipoproteinemia → E78.6
- Bassen-Kornzweig disease or syndrome → E78.6
- Hypoalphalipoproteinemia → E78.6
- Hypobetalipoproteinemia (familial) → E78.6
- Hypolipoproteinemia (alpha) (beta) → E78.6
- Tangier disease → E78.6
- Barth syndrome → E78.71
- Smith-Lemli-Opitz syndrome → E78.72
- Dermatoarthritis, lipoid → E78.81
- Lipogranulomatosis → E78.89
- Urbach's lipoid proteinosis → E78.89
- Urbach-Wiethe disease → E78.89
- Lipoprotein metabolism disorder → E78.9
- Osteochondrodystrophy → E78.9
- Cholesterol›elevated (high) → E78.00
- Elevated, elevation›cholesterol → E78.00
- Frederickson's hyperlipoproteinemia, type›IIA → E78.00
- High›cholesterol → E78.00
- Hyperlipoproteinemia›low-density-lipoprotein-type (LDL) → E78.00
- Xanthoma (s), xanthomatosis (primary) (familial) (hereditary)›hypercholesterinemic → E78.00
- Xanthoma (s), xanthomatosis (primary) (familial) (hereditary)›hypercholesterolemic → E78.00
- Cholesterolemia (essential) (pure)›familial → E78.019
- Cholesterolemia (essential) (pure)›hereditary → E78.019
- Hypercholesterolemia (essential) (primary) (pure)›familial → E78.019
- Hypercholesterolemia (essential) (primary) (pure)›hereditary → E78.019
- Disease, diseased›Bürger-Grütz (essential familial hyperlipemia) → E78.3
- Disease, diseased›chylomicron retention → E78.3
- Frederickson's hyperlipoproteinemia, type›I and V → E78.3
55 more, longer entries are not listed; the search box finds them by word.
NCHS Alphabetic Index. Index first, then the Tabular List.