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Q17.2 ICD-10-CM Code: Microtia

Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.

Coding at a Glance

Tabular directives
2 Excludes1 · 7 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 154 — OTHER EAR, NOSE, MOUTH AND THROAT DIAGNOSES WITH MCC (MDC 03)
  • MS-DRG 155 — OTHER EAR, NOSE, MOUTH AND THROAT DIAGNOSES WITH CC (MDC 03)
  • MS-DRG 156 — OTHER EAR, NOSE, MOUTH AND THROAT DIAGNOSES 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 Q17.2 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 Q17.2 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).

Source: inherited from Q17

Excludes2 — Not Included Here

Conditions not covered by this code, but which may be reported alongside it when both are present.

Source: inherited from Q10-Q18

Coder workflow for Q17.2

MedCoder structured workflow — derived from this code’s own official record

Before you code Q17.2

  1. Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q17.2. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).

    See the official tabular notes

Choose the right path

  1. Does the documentation support a condition named in Q17.2’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.

    ReviewQ18.1

Consider Q17.2. 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).

Official instructions as workflow

  • Excludes1 — check before selecting Q17.2(2 notes)

    Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q17.2: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.

    CompareQ18.1

    See the official tabular notes · Guidelines I.A.12.a

  • Excludes2 — not part of Q17.2(7 notes)

    Coding workflow: The conditions named in this note are not included in Q17.2. 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 Q17.2 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).

ReviewQ18.1

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

Microtia is a billable ICD-10-CM diagnosis code (Q17.2).

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 (3)

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

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 154 (MDC 03), DRG 155 (MDC 03), DRG 156 (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).

Q15.9 — Congenital malformation of eye, unspecified, Q16.0 — Congenital absence of (ear) auricle, Q16.1 — Congenital absence, atresia and stricture of auditory canal (external), Q16.2 — Absence of eustachian tube, Q16.3 — Congenital malformation of ear ossicles, 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, Q17.3 — 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, +41 more

Same Index main term, other category

The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Malformation”, “Hypoplasia, hypoplastic”; these codes share that main term but sit in a different category of the Tabular List.

Q14.3 — Congenital malformation of choroid (choroid), Q15.8 — Other specified congenital malformations of eye (eye, specified NEC), Q15.9 — Congenital malformation of eye, unspecified (eye), Q16.0 — Congenital absence of (ear) auricle (ear, external, causing impairment of hearing, absence of, auricle), Q16.1 — Congenital absence, atresia and stricture of auditory canal (external) (ear, external, causing impairment of hearing, absence of, auditory canal), Q16.2 — Absence of eustachian tube (ear, middle, absence of eustachian tube), Q16.3 — Congenital malformation of ear ossicles (ear, ossicles), Q16.4 — Other congenital malformations of middle ear (middle ear), Q16.5 — Congenital malformation of inner ear (cochlea), Q16.9 — Congenital malformation of ear causing impairment of hearing, unspecified (ear, causing impairment of hearing), Q18.2 — Other branchial cleft malformations (branchial cleft), Q18.8 — Other specified congenital malformations of face and neck (face), Q20.8 — Other congenital malformations of cardiac chambers and connections (cardiac, chambers, specified type NEC), Q20.9 — Congenital malformation of cardiac chambers and connections, unspecified (cardiac, chambers), Q21.8 — Other congenital malformations of cardiac septa (cardiac, septum, specified type NEC), Q21.9 — Congenital malformation of cardiac septum, unspecified (cardiac, septum), Q22.3 — Other congenital malformations of pulmonary valve (pulmonary, valve), Q22.6 — Hypoplastic right heart syndrome (right heart syndrome), Q22.8 — Other congenital malformations of tricuspid valve (tricuspid valve, specified type NEC), Q22.9 — Congenital malformation of tricuspid valve, unspecified (tricuspid valve), +218 more

Contextual Map

Every relationship of Q17.2 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.

Hierarchy

Clinical classification (CCSR)

MS-DRG Grouper

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

  • Hypoplasia, hypoplastic, ear (auricle) (lobe)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Malformation (congenital), ear, external, microtia[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
  • Microtia (congenital) (external ear)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026

Nearest codes

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. "Q17.2 — Microtia." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/q17.2-microtia

Change history

  • FY2016 — October 1, 2015
    In the code set at ICD-10-CM adoption
    Microtia

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 Q17.2 in its code family, with their registry titles.

View all codes in the Q17 family