E80.2 ICD-10-CM Code: Other and unspecified porphyria
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Coding at a Glance
- Tabular directives
- 1 inclusion term · 5 Excludes1 · 1 Excludes2
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E80.2 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 E80.2 itself; “inherited from” names the category or block whose note applies here.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- defects of catalase and peroxidase
Source: inherited from E80
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).
- androgen insensitivity syndrome (E34.5-) Compare E80.2 vs E34.5 →
- congenital adrenal hyperplasia (E25.0) Compare E80.2 vs E25.0 →
- hemolytic anemias attributable to enzyme disorders (D55.-) Compare E80.2 vs D55 →
- Marfan syndrome (Q87.4-) Compare E80.2 vs Q87.4 →
- 5-alpha-reductase deficiency (E29.1) Compare E80.2 vs E29.1 →
Source: inherited from E70-E88
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 E80.2 vs Q79.6 →
Source: inherited from E70-E88
Coder workflow for E80.2
MedCoder structured workflow — derived from this code’s own official record
Before you code E80.2
- E80.2 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).
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Unspecified does not mean incorrect. When the record gives no greater specificity, E80.2 may be the appropriate code. Check the record for detail that supports a more specific sibling. An unspecified code is for records that do not provide the detail a more specific code needs; a query, not an assumption, is the route to specificity (Guidelines I.A.9.b, I.B.18).
ReviewE80.0, E80.1, E80.3, E80.4, E80.5, E80.6
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E80.2. 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 E80.2?
Yes → Select that code and continue the checks below on its own page.
No → E80.2 cannot be reported as written; query for the specificity its subcategory needs. - Does the record document the detail a more specific sibling code needs?
Yes → Review the specific siblings in this subcategory.
No → Continue — E80.2 is appropriate when the documentation goes no further. - Does the documentation support a condition named in E80.2’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 E80.2. 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).
- Any detail beyond this code’s title
- What the record states that a more specific sibling code would capture — or its absence, which itself supports the unspecified code.
Official instructions as workflow
Excludes1 — check before selecting E80.2(5 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E80.2: 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 E80.2(1 note)
Coding workflow: The conditions named in this note are not included in E80.2. 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: The provider documents the condition in the terms of this code’s title and records no further detail.
Coding question: Is a more specific sibling code supportable?
Path: Review the specific siblings in this subcategory and what each requires the record to state.
Reason: A more specific code needs documentation of the distinguishing element; without it the unspecified code is appropriate, and a provider query is the route to specificity (Guidelines I.A.9.b, I.B.18).
Documentation: Both the condition E80.2 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.
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
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 structured relationships — computed from published CMS and AHRQ datasets
Other codes that name E80.2 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 (via E80.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 4 Excludes2 notes across 2 chapters: G11 — Hereditary ataxia (via E80.-), G71 — Primary disorders of muscles (via E80.-), N25.0 — Renal osteodystrophy (via E80.-), N25.81 — Secondary hyperparathyroidism of renal origin (via E80.-).
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 (via E80.-), H42 — Glaucoma in diseases classified elsewhere (via E80.-).
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 E80.2 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 E80.2 with these 7 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
Referenced by Excludes1 notes
- P59 — Neonatal jaundice from other and unspecified causes[Excludes1](via E80.-): “jaundice due to inborn errors of metabolism (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Excludes2 notes
- G11 — Hereditary ataxia[Excludes2](via E80.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- G71 — Primary disorders of muscles[Excludes2](via E80.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- N25.0 — Renal osteodystrophy[Excludes2](via E80.-): “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- N25.81 — Secondary hyperparathyroidism of renal origin[Excludes2](via E80.-): “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code First instructions
- G63 — Polyneuropathy in diseases classified elsewhere[Code First](via E80.-): “metabolic diseases (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- H42 — Glaucoma in diseases classified elsewhere[Code First](via E80.-): “specified metabolic disorder (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Nearest codes (11)
- E80 — Disorders of porphyrin and bilirubin metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.0 — Hereditary erythropoietic porphyria[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.1 — Porphyria cutanea tarda[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.20 — Unspecified porphyria[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.21 — Acute intermittent (hepatic) porphyria[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.29 — Other porphyria[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.3 — Defects of catalase and peroxidase[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E80.4 — Gilbert syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 3 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Common coding questions
Can E80.2 be billed directly?
No. E80.2 (Other and unspecified porphyria) 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 structured 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 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.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
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. "E80.2 — Other and unspecified porphyria." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/e80.2-other-and-unspecified-porphyria
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionOther and unspecified porphyria
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 E80.2 in its code family, with their registry titles.
- E80 — Disorders of porphyrin and bilirubin metabolism
- E80.0 — Hereditary erythropoietic porphyria
- E80.1 — Porphyria cutanea tarda
- E80.20 — Unspecified porphyria
- E80.21 — Acute intermittent (hepatic) porphyria
- E80.29 — Other porphyria
- E80.3 — Defects of catalase and peroxidase
- E80.4 — Gilbert syndrome
- E80.5 — Crigler-Najjar syndrome
- E80.6 — Other disorders of bilirubin metabolism