Q81.8 ICD-10-CM Code: Other epidermolysis bullosa
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v44, Appendix B.
- MS-DRG 595 — MAJOR SKIN DISORDERS WITH MCC (MDC 09)
- MS-DRG 596 — MAJOR SKIN DISORDERS WITHOUT MCC (MDC 09)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Coder workflow for Q81.8
MedCoder structured workflow — derived from this code’s own official record
Before you code Q81.8
- “Other” (NEC) means the condition is specified in the record but no dedicated code captures it. Confirm the documented form is not one a sibling code names before settling on Q81.8; if the record states no specifics at all, the unspecified sibling applies instead. “Other” codes are for documented conditions the classification gives no specific code; “unspecified” codes are for records lacking the detail (Guidelines I.A.9.a, I.A.9.b).
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
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.
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.
Indexed Clinical Terms (4)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
Verify Before Coding
- No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.
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 Q81.8 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 2 Excludes1 notes across 2 chapters: L12.3 — Acquired epidermolysis bullosa (via Q81.-), P83 — Other conditions of integument specific to newborn (via Q81.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
MS-DRG Grouper Relationships (FY2027)
Potential MS-DRG participation — not a DRG assignment.
FY2027 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.
Named in the grouper logic of 2 MS-DRGs: DRG 595 (MDC 09), DRG 596 (MDC 09).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL010 — Other specified and unspecified congenital anomalies (default).
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other specified and unspecified congenital anomalies).
Q80.0 — Ichthyosis vulgaris, Q80.1 — X-linked ichthyosis, Q80.2 — Lamellar ichthyosis, Q80.3 — Congenital bullous ichthyosiform erythroderma, Q80.4 — Harlequin fetus, Q80.8 — Other congenital ichthyosis, Q80.9 — Congenital ichthyosis, unspecified, Q81.0 — Epidermolysis bullosa simplex, Q81.1 — Epidermolysis bullosa letalis, Q81.2 — Epidermolysis bullosa dystrophica, Q81.9 — Epidermolysis bullosa, unspecified, Q82.0 — Hereditary lymphedema, Q82.1 — Xeroderma pigmentosum, Q82.2 — Congenital cutaneous mastocytosis, Q82.3 — Incontinentia pigmenti, Q82.4 — Ectodermal dysplasia (anhidrotic), Q82.5 — Congenital non-neoplastic nevus, Q82.6 — Congenital sacral dimple, Q82.8 — Other specified congenital malformations of skin, Q82.9 — Congenital malformation of skin, unspecified, +59 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Epidermolysis”; these codes share that main term but sit in a different category of the Tabular List.
L12.30 — Acquired epidermolysis bullosa, unspecified (bullosa, acquired), L12.31 — Epidermolysis bullosa due to drug (bullosa, acquired, drug-induced), L12.35 — Other acquired epidermolysis bullosa (bullosa, acquired, specified cause NEC), L51.2 — Toxic epidermal necrolysis [Lyell] (necroticans combustiformis)
Contextual Map
Every relationship of Q81.8 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 Q81.8 with these 2 related codes in Claim Check
Hierarchy
- Q00-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q80-Q89 — Other congenital malformations[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes1 notes
- L12.3 — Acquired epidermolysis bullosa[Excludes1](via Q81.-): “epidermolysis bullosa (congenital) (Q81.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- P83 — Other conditions of integument specific to newborn[Excludes1](via Q81.-): “congenital malformations of skin and integument (Q80-Q84)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Clinical classification (CCSR)
- MAL010 — Other specified and unspecified congenital anomalies[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 595 — MAJOR SKIN DISORDERS WITH MCC[MS-DRG]: “MAJOR SKIN DISORDERS WITH MCC (MDC 09)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 596 — MAJOR SKIN DISORDERS WITHOUT MCC[MS-DRG]: “MAJOR SKIN DISORDERS WITHOUT MCC (MDC 09)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
MDC crossing
- MDC 09 — Diseases and Disorders of the Skin, Subcutaneous Tissue and Breast[MDC crossing]: “Diseases and Disorders of the Skin, Subcutaneous Tissue and Breast — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 7,378 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries
- Epidermolysis, bullosa (congenital), specified NEC[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Goldscheider's disease[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Köebner's syndrome[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Weber-Cockayne syndrome (epidermolysis bullosa)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes
- Q81 — Epidermolysis bullosa[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q81.0 — Epidermolysis bullosa simplex[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q81.1 — Epidermolysis bullosa letalis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q81.2 — Epidermolysis bullosa dystrophica[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q81.9 — Epidermolysis bullosa, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
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
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v44 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. "Q81.8 — Other epidermolysis bullosa." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q81.8-other-epidermolysis-bullosa
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionOther epidermolysis bullosa
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 Q81.8 in its code family, with their registry titles.