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Q30.1 ICD-10-CM Code: Agenesis and underdevelopment of nose

Compare with another code for Q30.1Check this code on a claim

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

Coding at a Glance

Tabular directives
1 inclusion term · 1 Excludes1

Billable · FY2027A valid, specific ICD-10-CM code, reportable for dates of service in FY2027.

What you need to know

Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too, and is marked with where it comes from.

Excludes1from Q30Never report with this code
  • congenital deviation of nasal septum (Q67.4)
IncludesWhat this code covers
  • Congenital absent of nose

Where it sits Source: CMS/NCHS

Under:Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)Q30-Q34 Congenital malformations of the respiratory systemQ30 Congenital malformations of nose

Most relevant related codes MedCoder-derived

Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.

CompareCheck ClaimView Related Codes

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 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 Q30.1 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 Q30.1 itself; “inherited from” names the category or block whose note applies here.

Inclusion Terms

Alternative terms the tabular list files under this code.

  • Congenital absent of nose

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 Q30

Coder workflow for Q30.1

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

Before you code Q30.1

  1. Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with Q30.1. 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 Q30.1’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.

    ReviewQ67.4

Consider Q30.1. 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 Q30.1(1 note)

    Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with Q30.1: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.

    CompareQ67.4

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

Coding decision scenarios

Pattern scenarios for this code’s structure — decision rules, not clinical cases

Documentation: Both the condition Q30.1 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).

ReviewQ67.4

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.

Don’t confuse Q30.1 with…

MedCoder analysis — pairs from this code’s official notes, distinctions written by MedCoder

The codes most likely to be picked instead of Q30.1 — named in its own official notes, or sharing its laterality or encounter family — with what separates them and which documentation moves the case. Each links to the full comparison.

  • Q67.4— Excludes1 conflict (Excludes1 — generally not reported together)

    Not coded here — the tabular list excludes this pair for the same encounter.

    Not reported together with this code, except where the two conditions are documented as unrelated.

    What moves you there: Documentation of congenital deviation of nasal septum moves the case to Q67.4; the two are not reported together unless documented as unrelated.

    Full comparison: Q30.1 vs Q67.4 →

  • Q30.9— Specificity relationship (Review)

    Overlapping diagnoses in the same category.

    Overlapping codes in the same category — the documentation decides which is the more specific fit.

    What moves you there: A record that documents no more than “Congenital malformation of nose, unspecified” takes Q30.9; specificity in the record moves it back here.

    Full comparison: Q30.1 vs Q30.9 →

Relationships are read from this code's own official notes, its laterality siblings and its encounter family; the wording of each distinction is MedCoder editorial, and the documentation named in each “what moves you there” line is the official note phrase or sibling title itself. Source: CMS ICD-10-CM tabular instructional notes; ICD-10-CM Official Guidelines, Section I.A.12.a.

Coding context

Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.

Code Overview

Agenesis and underdevelopment of nose is a billable ICD-10-CM diagnosis code (Q30.1).

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

  • 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-derived relationships — computed from published CMS and AHRQ datasets

Other codes that name Q30.1 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 10 Excludes2 notes: Q10 — Congenital malformations of eyelid, lacrimal apparatus and orbit (via Q30.-), Q10-Q18 — Congenital malformations of eye, ear, face and neck (Q10-Q18) (via Q30.-), Q11 — Anophthalmos, microphthalmos and macrophthalmos (via Q30.-), Q12 — Congenital lens malformations (via Q30.-), Q13 — Congenital malformations of anterior segment of eye (via Q30.-), Q14 — Congenital malformations of posterior segment of eye (via Q30.-), Q15 — Other congenital malformations of eye (via Q30.-), Q16 — Congenital malformations of ear causing impairment of hearing (via Q30.-), Q17 — Other congenital malformations of ear (via Q30.-), Q18 — Other congenital malformations of face and neck (via Q30.-).

These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.

Referenced by 1 Code Also instruction: P28 — Other respiratory conditions originating in the perinatal period (via Q30.-).

These codes suggest coding this condition alongside when both are present.

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 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):MAL007 — Respiratory congenital malformations (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 (Respiratory congenital malformations).

Q30.0 — Choanal atresia, Q30.2 — Fissured, notched and cleft nose, Q30.3 — Congenital perforated nasal septum, Q30.8 — Other congenital malformations of nose, Q30.9 — Congenital malformation of nose, unspecified, Q31.0 — Web of larynx, Q31.1 — Congenital subglottic stenosis, Q31.2 — Laryngeal hypoplasia, Q31.3 — Laryngocele, Q31.5 — Congenital laryngomalacia, Q31.8 — Other congenital malformations of larynx, Q31.9 — Congenital malformation of larynx, unspecified, Q32.0 — Congenital tracheomalacia, Q32.1 — Other congenital malformations of trachea, Q32.2 — Congenital bronchomalacia, Q32.3 — Congenital stenosis of bronchus, Q32.4 — Other congenital malformations of bronchus, Q33.0 — Congenital cystic lung, Q33.1 — Accessory lobe of lung, Q33.2 — Sequestration of lung, +10 more

Same Index main term, other category

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

Q25.79 — Other congenital malformations of pulmonary artery (artery, pulmonary), Q26.5 — Anomalous portal venous connection (vein, portal), Q26.8 — Other congenital malformations of great veins (vena cava), Q27.0 — Congenital absence and hypoplasia of umbilical artery (artery, umbilical), Q27.8 — Other specified congenital malformations of peripheral vascular system (artery), Q27.9 — Congenital malformation of peripheral vascular system, unspecified (vein), Q28.1 — Other malformations of precerebral vessels (veincongenital NEC, precerebral), Q28.3 — Other malformations of cerebral vessels (vein, brain), Q28.8 — Other specified congenital malformations of circulatory system (ductus arteriosus), Q28.9 — Congenital malformation of circulatory system, unspecified (circulatory system, part NOS), Q31.2 — Laryngeal hypoplasia (larynx), Q31.8 — Other congenital malformations of larynx (larynx), Q32.1 — Other congenital malformations of trachea (trachea), Q32.4 — Other congenital malformations of bronchus (bronchus), Q33.3 — Agenesis of lung (lung), Q33.6 — Congenital hypoplasia and dysplasia of lung (lung), Q34.8 — Other specified congenital malformations of respiratory system (respiratory organ NEC), Q34.9 — Congenital malformation of respiratory system, unspecified (respiratory organ NOS), Q38.0 — Congenital malformations of lips, not elsewhere classified (lip), Q38.3 — Other congenital malformations of tongue (tongue), +256 more

Contextual Map

Every relationship of Q30.1 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 Q30.1 with these 9 related codes in Claim Check

Hierarchy

Referenced by Excludes2 notes (10)

Referenced by Code Also instructions

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. 5,151 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027

Index entries

  • Absence (of) (organ or part) (complete or partial), nose (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Agenesis, nose[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Hypoplasia, hypoplastic, nose, nasal[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
  • Underdevelopment, nose[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027

Nearest codes

Change history

  • FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016

Reference

Index terms and tables, published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.

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.

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-derived 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 editorial 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.

Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources

Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules

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. "Q30.1 — Agenesis and underdevelopment of nose." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q30.1-agenesis-and-underdevelopment-of-nose

Change history

  • FY2016 — October 1, 2015
    In the code set at ICD-10-CM adoption
    Agenesis and underdevelopment of nose

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 Q30.1 in its code family, with their registry titles.

View all codes in the Q30 family