E78 ICD-10-CM Code: Disorders of lipoprotein metabolism and other lipidemias
Compare with another codeCheck this code on a claim
Billing Status: NO. This is a non-billable ICD-10-CM code: report a more specific billable code beneath it.
Coding at a Glance
- Tabular directives
- 6 Excludes1 · 1 Excludes2
Category · FY2027A non-billable heading in the tabular list: report a more specific code beneath it.
What you need to know
Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too; the Instructions section marks which is which.
- Excludes1Never report with this code
- Excludes2Not included here; may be reported together
- Ehlers-Danlos syndromes (Q79.6-)
Most relevant related codes MedCoder-derived
- E78.0Pure hypercholesterolemiaMore specific code
- E78.00Pure hypercholesterolemia, unspecifiedMore specific code
- E78.01Familial hypercholesterolemiaMore specific code
- E78.010Homozygous familial hypercholesterolemia [HoFH]More specific code
- E78.011Heterozygous familial hypercholesterolemia [HeFH]More specific code
- E78.019Familial hypercholesterolemia, unspecifiedMore specific code
Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E78 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Trace:FY2027 changesChange historyRelease, file and checksum
Notes without a marker are published on E78 itself; “inherited from” names the category or block whose note applies here.
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- sphingolipidosis (E75.0-E75.3) Compare E78 vs E75.0 →
- androgen insensitivity syndrome (E34.5-) inherited from E70-E88Compare E78 vs E34.5 →
- congenital adrenal hyperplasia (E25.0) inherited from E70-E88Compare E78 vs E25.0 →
- hemolytic anemias attributable to enzyme disorders (D55.-) inherited from E70-E88Compare E78 vs D55 →
- Marfan syndrome (Q87.4-) inherited from E70-E88Compare E78 vs Q87.4 →
- 5-alpha-reductase deficiency (E29.1) inherited from E70-E88Compare E78 vs E29.1 →
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- Ehlers-Danlos syndromes (Q79.6-) Compare E78 vs Q79.6 →
Source: inherited from E70-E88
Coder workflow for E78
MedCoder structured workflow — derived from this code’s own official record
Before you code E78
- E78 is not reportable as written. Select the more specific code beneath it that the documentation supports. Codes are reported to the highest level of specificity the classification provides (Guidelines I.B.2).
ReviewE78.0, E78.1, E78.2, E78.3, E78.4, E78.5, E78.6, E78.7, E78.8, E78.9
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E78. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support one of the more specific codes beneath E78?
Yes → Select that code and continue the checks below on its own page.
No → E78 cannot be reported as written; query for the specificity its subcategory needs.ReviewE78.0, E78.1, E78.2, E78.3, E78.4, E78.5, E78.6, E78.7, E78.8, E78.9
- Does the documentation support a condition named in E78’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider E78. Then confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
Official instructions as workflow
Excludes1 — check before selecting E78(6 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E78: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareE34.5, E25.0, D55, Q87.4, E29.1
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of E78(1 note)
Coding workflow: The conditions named in this note are not included in E78. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareQ79.6
See the official tabular notes · Guidelines I.A.12.b
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition E78 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Coding context
Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Verify Before Coding
- Not billable as written — a more specific code is required: E78.00, E78.010, E78.011, E78.019, E78.1.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder-derived relationships — computed from published CMS and AHRQ datasets
Other codes that name E78 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 1 Excludes1 note: P59 — Neonatal jaundice from other and unspecified causes.
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 15 Excludes2 notes across 4 chapters: E88.0 — Disorders of plasma-protein metabolism, not elsewhere classified, G11 — Hereditary ataxia, G71 — Primary disorders of muscles, N25.0 — Renal osteodystrophy, N25.81 — Secondary hyperparathyroidism of renal origin, R70 — Elevated erythrocyte sedimentation rate and abnormality of plasma viscosity, R70-R79 — Abnormal findings on examination of blood, without diagnosis (R70-R79), R71 — Abnormality of red blood cells, R73 — Elevated blood glucose level, R74 — Abnormal serum enzyme levels, R75 — Inconclusive laboratory evidence of human immunodeficiency virus [HIV], R76 — Other abnormal immunological findings in serum, R77 — Other abnormalities of plasma proteins, R78 — Findings of drugs and other substances, not normally found in blood, R79 — Other abnormal findings of blood chemistry.
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 2 Code First instructions across 2 chapters: G63 — Polyneuropathy in diseases classified elsewhere, H42 — Glaucoma in diseases classified elsewhere.
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
Contextual Map
Every relationship of E78 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run E78 with these 18 related codes in Claim Check
Hierarchy
- E00-E89 — Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89) (E00-E89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E70-E88 — Metabolic disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Excludes1
- D55 — Anemia due to enzyme disorders[Excludes1]: “hemolytic anemias attributable to enzyme disorders (D55.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- E25.0 — Congenital adrenogenital disorders associated with enzyme deficiency[Excludes1]: “congenital adrenal hyperplasia (E25.0)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- E29.1 — Testicular hypofunction[Excludes1]: “5-alpha-reductase deficiency (E29.1)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- E34.5 — Androgen insensitivity syndrome[Excludes1]: “androgen insensitivity syndrome (E34.5-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- E75 — Disorders of sphingolipid metabolism and other lipid storage disorders[Excludes1]: “sphingolipidosis (E75.0-E75.3)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- Q87.4 — Marfan syndrome[Excludes1]: “Marfan syndrome (Q87.4-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Excludes2
- Q79.6 — Ehlers-Danlos syndromes[Excludes2]: “Ehlers-Danlos syndromes (Q79.6-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Excludes1 notes
- P59 — Neonatal jaundice from other and unspecified causes[Excludes1]: “jaundice due to inborn errors of metabolism (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Excludes2 notes (15)
- E88.0 — Disorders of plasma-protein metabolism, not elsewhere classified[Excludes2]: “disorder of lipoprotein metabolism (E78.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- G11 — Hereditary ataxia[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- G71 — Primary disorders of muscles[Excludes2]: “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- N25.0 — Renal osteodystrophy[Excludes2]: “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- N25.81 — Secondary hyperparathyroidism of renal origin[Excludes2]: “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R70 — Elevated erythrocyte sedimentation rate and abnormality of plasma viscosity[Excludes2]: “abnormalities of lipids (E78.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R70-R79 — Abnormal findings on examination of blood, without diagnosis (R70-R79)[Excludes2]: “abnormalities of lipids (E78.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R71 — Abnormality of red blood cells[Excludes2]: “abnormalities of lipids (E78.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- and 7 more
Referenced by Code First instructions
- G63 — Polyneuropathy in diseases classified elsewhere[Code First]: “metabolic diseases (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- H42 — Glaucoma in diseases classified elsewhere[Code First]: “specified metabolic disorder (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Nearest codes (23)
- E78.0 — Pure hypercholesterolemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.00 — Pure hypercholesterolemia, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.01 — Familial hypercholesterolemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.010 — Homozygous familial hypercholesterolemia [HoFH][Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.011 — Heterozygous familial hypercholesterolemia [HeFH][Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.019 — Familial hypercholesterolemia, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.1 — Pure hyperglyceridemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E78.2 — Mixed hyperlipidemia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 15 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Reference
Index terms and tables, published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.
Common coding questions
MedCoder editorial
Can E78 be billed directly?
No. E78 (Disorders of lipoprotein metabolism and other lipidemias) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v44.0 (October 2026) Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder-derived relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder editorial explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources
Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "E78 — Disorders of lipoprotein metabolism and other lipidemias." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/e78-disorders-of-lipoprotein-metabolism-and-other-lipidemias
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionDisorders of lipoprotein metabolism and other lipidemias
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027, and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to E78 in its code family, with their registry titles.
- E78.0 — Pure hypercholesterolemia
- E78.00 — Pure hypercholesterolemia, unspecified
- E78.01 — Familial hypercholesterolemia
- E78.010 — Homozygous familial hypercholesterolemia [HoFH]
- E78.011 — Heterozygous familial hypercholesterolemia [HeFH]
- E78.019 — Familial hypercholesterolemia, unspecified
- E78.1 — Pure hyperglyceridemia
- E78.2 — Mixed hyperlipidemia
- E78.3 — Hyperchylomicronemia
- E78.4 — Other hyperlipidemia
- E78.41 — Elevated Lipoprotein(a)
- E78.49 — Other hyperlipidemia
- E78.5 — Hyperlipidemia, unspecified
- E78.6 — Lipoprotein deficiency
- E78.7 — Disorders of bile acid and cholesterol metabolism
- E78.70 — Disorder of bile acid and cholesterol metabolism, unspecified
- E78.71 — Barth syndrome
- E78.72 — Smith-Lemli-Opitz syndrome
- E78.79 — Other disorders of bile acid and cholesterol metabolism
- E78.8 — Other disorders of lipoprotein metabolism
- E78.81 — Lipoid dermatoarthritis
- E78.89 — Other lipoprotein metabolism disorders
- E78.9 — Disorder of lipoprotein metabolism, unspecified