Q18.5 ICD-10-CM Code: Microstomia
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 7 Excludes1 · 6 Excludes2
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 v43, Appendix B.
- MS-DRG 157 — DENTAL AND ORAL DISEASES WITH MCC (MDC 03)
- MS-DRG 158 — DENTAL AND ORAL DISEASES WITH CC (MDC 03)
- MS-DRG 159 — DENTAL AND ORAL DISEASES WITHOUT CC/MCC (MDC 03)
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.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for Q18.5 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on Q18.5 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).
- cleft lip and cleft palate (Q35-Q37) inherited from Q18Compare Q18.5 vs Q35 →
- conditions classified to Q67.0-Q67.4 inherited from Q18
- congenital malformations of skull and face bones (Q75.-) inherited from Q18Compare Q18.5 vs Q75 →
- cyclopia (Q87.0) inherited from Q18Compare Q18.5 vs Q87.0 →
- dentofacial anomalies including malocclusion
- malformation syndromes affecting facial appearance (Q87.0) inherited from Q18Compare Q18.5 vs Q87.0 →
- persistent thyroglossal duct (Q89.2) inherited from Q18Compare Q18.5 vs Q89.2 →
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4) Compare Q18.5 vs Q05.0 →
- congenital malformation of larynx (Q31.-) Compare Q18.5 vs Q31 →
- congenital malformation of lip NEC (Q38.0) Compare Q18.5 vs Q38.0 →
- congenital malformation of nose (Q30.-) Compare Q18.5 vs Q30 →
- congenital malformation of parathyroid gland (Q89.2) Compare Q18.5 vs Q89.2 →
- congenital malformation of thyroid gland (Q89.2) Compare Q18.5 vs Q89.2 →
Source: inherited from Q10-Q18
Coder workflow for Q18.5
MedCoder structured workflow — derived from this code’s own official record
Before you code Q18.5
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q18.5. 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 a condition named in Q18.5’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 Q18.5. 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 Q18.5(7 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q18.5: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of Q18.5(6 notes)
Coding workflow: The conditions named in this note are not included in Q18.5. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareQ05.0, Q05.5, Q67.5, Q31, Q38.0, Q30
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 Q18.5 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.
Indexed Clinical Terms (1)
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 Q18.5 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: Q38 — Other congenital malformations of tongue, mouth and pharynx, Q75 — Other congenital malformations of skull and face bones (via Q18.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 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 3 MS-DRGs: DRG 157 (MDC 03), DRG 158 (MDC 03), DRG 159 (MDC 03).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):MAL005 — Congenital malformations of eye, ear, face, neck (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 (Congenital malformations of eye, ear, face, neck).
Q16.4 — Other congenital malformations of middle ear, Q16.5 — Congenital malformation of inner ear, Q16.9 — Congenital malformation of ear causing impairment of hearing, unspecified, Q17.0 — Accessory auricle, Q17.1 — Macrotia, Q17.2 — Microtia, Q17.3 — Other misshapen ear, Q17.4 — Misplaced ear, Q17.5 — Prominent ear, Q17.8 — Other specified congenital malformations of ear, Q17.9 — Congenital malformation of ear, unspecified, Q18.0 — Sinus, fistula and cyst of branchial cleft, Q18.1 — Preauricular sinus and cyst, Q18.2 — Other branchial cleft malformations, Q18.3 — Webbing of neck, Q18.4 — Macrostomia, Q18.6 — Macrocheilia, Q18.7 — Microcheilia, Q18.8 — Other specified congenital malformations of face and neck, Q18.9 — Congenital malformation of face and neck, unspecified, +41 more
Contextual Map
Every relationship of Q18.5 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 Q18.5 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-fy2026
- Q10-Q18 — Congenital malformations of eye, ear, face and neck[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Referenced by Excludes1 notes
- Q38 — Other congenital malformations of tongue, mouth and pharynx[Excludes1]: “microstomia (Q18.5)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- Q75 — Other congenital malformations of skull and face bones[Excludes1](via Q18.-): “congenital malformation of face NOS (Q18.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Clinical classification (CCSR)
- MAL005 — Congenital malformations of eye, ear, face, neck[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 157 — DENTAL AND ORAL DISEASES WITH MCC[MS-DRG]: “DENTAL AND ORAL DISEASES WITH MCC (MDC 03)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 158 — DENTAL AND ORAL DISEASES WITH CC[MS-DRG]: “DENTAL AND ORAL DISEASES WITH CC (MDC 03)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 159 — DENTAL AND ORAL DISEASES WITHOUT CC/MCC[MS-DRG]: “DENTAL AND ORAL DISEASES WITHOUT CC/MCC (MDC 03)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 03 — Diseases and Disorders of the Ear, Nose, Mouth and Throat[MDC crossing]: “Diseases and Disorders of the Ear, Nose, Mouth and Throat — 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. 5,147 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries
- Microstomia (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
Nearest codes (10)
- Q18 — Other congenital malformations of face and neck[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.0 — Sinus, fistula and cyst of branchial cleft[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.1 — Preauricular sinus and cyst[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.2 — Other branchial cleft malformations[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.3 — Webbing of neck[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.4 — Macrostomia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.6 — Macrocheilia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- Q18.7 — Microcheilia[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 2 more
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 FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 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 — v43 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. "Q18.5 — Microstomia." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/q18.5-microstomia
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionMicrostomia
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), 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 Q18.5 in its code family, with their registry titles.
- Q18 — Other congenital malformations of face and neck
- Q18.0 — Sinus, fistula and cyst of branchial cleft
- Q18.1 — Preauricular sinus and cyst
- Q18.2 — Other branchial cleft malformations
- Q18.3 — Webbing of neck
- Q18.4 — Macrostomia
- Q18.6 — Macrocheilia
- Q18.7 — Microcheilia
- Q18.8 — Other specified congenital malformations of face and neck
- Q18.9 — Congenital malformation of face and neck, unspecified