M26.06 identifies microgenia — an abnormally small or underdeveloped chin (symphysis menti region of the mandible) classified as a major anomaly of jaw size under the dentofacial anomalies category.
Verified May 8, 2026 · 4 sources ↓
- Status
- Billable
- Chapter
- 13
- Related CPT
- 5
- Region
- Other
Documentation tips
What should appear in the chart to support M26.06.
Source · Editorial brief grounded in 4 cited references ↓
- Document 'microgenia' explicitly — vague terms like 'small chin' or 'chin deficiency' may not map cleanly to M26.06 on audit.
- Distinguish microgenia (chin region only) from mandibular hypoplasia (M26.04, affecting the whole mandible) in the clinical note; conflating the two can result in the wrong code.
- Record any associated dentofacial anomalies separately (e.g., malocclusion, jaw asymmetry) so each condition can be coded with its own specific code.
- If surgical planning is the purpose of the visit, document how microgenia specifically contributes to the functional or structural problem justifying the procedure.
- Rule out and explicitly exclude Robin syndrome (Q87.0) or acromegaly (E22.0) in the note when those diagnoses are in the differential — payers may flag co-reporting of these Excludes1 conditions.
Related CPT procedures
Procedure codes commonly billed with M26.06. Linking the right diagnosis to the right procedure is what establishes medical necessity.
Source · CMS LCDs · AAOS specialty guidance · claims-pattern analysis
Common coding pitfalls
The recurring mistakes coders make with M26.06 and adjacent codes.
Source · Editorial brief grounded in CDC ICD-10-CM tabular guidance, AAOS coding references, and cited references ↓
- Assigning M26.06 when Robin syndrome (Q87.0) is the underlying diagnosis — Q87.0 is an Excludes1 condition at the M26.0 category level, making simultaneous use of both codes a coding violation.
- Confusing M26.06 (microgenia, chin-specific) with M26.04 (mandibular hypoplasia, whole mandible) — these are clinically and structurally distinct; the provider's documented term controls the code selection.
- Using parent code M26.04 or M26.00 when the documentation clearly states microgenia — M26.06 is billable and specific; dropping to an unspecified code is unnecessary and may trigger a query.
- Omitting secondary dentofacial anomaly codes (e.g., malocclusion M26.2x) when they are documented — microgenia frequently coexists with other jaw-size or occlusal anomalies that should each be reported.
Clinical context
Source · Editorial summary grounded in 4 cited references ↓
M26.06 applies when a provider documents microgenia — a chin that is disproportionately small relative to the rest of the mandible and face. It sits under parent code M26.0 (Major anomalies of jaw size) and is distinct from mandibular hypoplasia (M26.04), which describes underdevelopment of the entire mandible. Microgenia specifically refers to the chin prominence itself, not the ramus or body of the mandible at large.
This code is used across oral and maxillofacial surgery, craniofacial plastic surgery, and orthodontic practices when microgenia is the documented diagnosis driving evaluation or surgical planning. Common clinical scenarios include genioplasty workup, orthognathic surgery planning, and orthodontic treatment coordination. It may be reported alongside malocclusion codes (M26.2x) or jaw-cranial base relationship codes (M26.1x) when those conditions coexist.
Two Excludes1 conditions apply at the M26.0 category level: acromegaly (E22.0) and Robin syndrome (Q87.0). If the small chin is a feature of Pierre Robin sequence, assign Q87.0 — not M26.06. Acromegaly-related jaw changes also cannot be coded here. These are hard exclusions, not optional choices.
Sibling codes
Other billable codes under M26.0 (laterality / anatomic variants).
Frequently asked questions
Source · Generated from the editorial pipeline, verified against 4 cited references ↓
01What is the difference between M26.06 (microgenia) and M26.04 (mandibular hypoplasia)?
02Can M26.06 and Q87.0 (Robin syndrome) be coded together?
03Is M26.06 used for congenital or acquired microgenia?
04Which CPT codes are typically paired with M26.06 for surgical cases?
05Can M26.06 be reported alongside malocclusion codes?
06Does M26.06 require a 7th character extension?
07Is M26.06 valid for FY2026 claims?
Sources & references
Editorial content was developed using the following public sources. Last verified May 8, 2026.
- 01CDC ICD-10-CM Tabular List 2026 (effective Oct 1, 2025)
- 02icd10data.comhttps://www.icd10data.com/ICD10CM/Codes/M00-M99/M26-M27/M26-/M26.06
- 03aapc.comhttps://www.aapc.com/codes/icd-10-codes/M26.06
- 04icd10data.comhttps://www.icd10data.com/ICD10CM/Codes/M00-M99/M26-M27/M26-
Mira AI Scribe
The Mira AI Scribe captures the provider's specific anatomical characterization of the chin (size, projection, symmetry), any imaging or cephalometric findings supporting the diagnosis, associated dentofacial anomalies, and explicit exclusion of Robin syndrome or acromegaly. This precision prevents downfall to the unspecified M26.00 and protects against Excludes1 audit flags.
See how Mira captures M26.06 documentation