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    OpenPayerBilling CodesCongenital malformations of the respiratory systemICD-10-CM q31-congenital-malformations-of-larynx
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    ICD-10-CM Code For Congenital Malformations Of Larynx: Group Overview

    The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group Q31 includes congenital anomalies of the larynx such as laryngeal atresia, laryngeal clefts, webs, and stenoses that impair airway, phonation, or swallowing. These ICD-10-CM diagnosis codes are used to document anatomical abnormalities present at birth, their severity, and any associated functional compromise or need for intervention. Accurate coding within the ICD-10-CM Q31 group supports proper claim adjudication, complete clinical documentation, and appropriate reimbursement.

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    ICD-10-CM Q31: Congenital Malformations Of Larynx Overview

    This group represents congenital structural anomalies of the larynx affecting airway patency, voice, and swallowing in newborns and children. These conditions are part of congenital malformations of the respiratory system and can range from minor webbing to severe atresia. Accurate coding matters for capturing clinical complexity and supporting appropriate claim processing and medical record completeness.

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    When to Use

    Assign a code from this group when a congenital laryngeal anomaly is diagnosed and documented in the medical record, whether identified prenatally, at birth, or during early childhood. Use these codes to capture the specific type of malformation and any documented functional impact on airway, voice, or swallowing.

    ICD-10-CM Codes

    7 rows

    ICD-10-CM CodeDescription
    Q31.0Web of larynx
    Q31.1Congenital subglottic stenosis
    Q31.2Laryngeal hypoplasia
    Q31.3Laryngocele
    Q31.5Congenital laryngomalacia
    Q31.8Other congenital malformations of larynx
    Q31.9Congenital malformation of larynx, unspecified

    DRG Codes

    6 rows

    DRG CodeDescription
    011Tracheostomy for Face, Mouth and Neck Diagnoses or Laryngectomy with MCC
    012Tracheostomy for Face, Mouth and Neck Diagnoses or Laryngectomy with CC
    013Tracheostomy for Face, Mouth and Neck Diagnoses or Laryngectomy without CC/MCC
    154Other Ear, Nose, Mouth and Throat Diagnoses with MCC
    155Other Ear, Nose, Mouth and Throat Diagnoses with CC
    156Other Ear, Nose, Mouth and Throat Diagnoses without CC/MCC

    Typical Clinical Scenarios

    • Neonatal respiratory distress due to anatomic airway obstruction: A newborn in the delivery room has stridor, cyanosis, and inspiratory respiratory distress not responsive to routine resuscitation; flexible laryngoscopy reveals a partial congenital laryngeal web occluding the glottic opening. The infant is admitted to the NICU for oxygen support and possible surgical airway evaluation; a congenital laryngeal web diagnosis from this group is assigned as the primary anatomic cause of the obstruction. Typical codes: Q31.2
    • Chronic noisy breathing and feeding difficulty in an infant with a known congenital laryngeal anomaly: A 6-month-old presents to ENT clinic for persistent inspiratory stridor, recurrent choking with feeds, and failure to thrive; prior imaging and endoscopy documented congenital laryngomalacia with supraglottic collapse. The visit documents ongoing management and monitoring of the congenital laryngeal abnormality as the underlying chronic condition, so a code for congenital malformation of the larynx is assigned. Typical codes: Q31.0, Q31.9
    • Adult presenting with progressive hoarseness and intermittent airway compromise attributed to a congenital laryngeal lesion identified incidentally: A 45-year-old with long-standing mild voice change develops progressive dysphonia and intermittent dyspnea; laryngoscopy reveals a congenital laryngeal cyst or submucosal lesion causing vocal fold impairment and occasional partial airway obstruction. The clinician documents the congenital laryngeal malformation as a contributing comorbidity to the current symptoms and plans for surgical evaluation, warranting assignment of a congenital larynx malformation code. Typical codes: Q31.3, Q31.8

    Related Codes

    Q30-CONGENITAL-MALFORMATIONS-OF-NOSE

    ICD-10-CM Code For Congenital Malformations Of Nose: Group Overview

    Q32-CONGENITAL-MALFORMATIONS-TRACHEA-BRONCHUS

    ICD-10-CM Code For Congenital Malformations Of Trachea And Bronchus: Group Overview

    Q33-CONGENITAL-MALFORMATIONS-OF-LUNG

    ICD-10-CM Code For Congenital Malformations Of Lung: Group Overview

    Q34-OTHER-CONGENITAL-RESPIRATORY-MALFORMATIONS

    ICD-10-CM Code For Other Congenital Malformations Of Respiratory System: Group Overview

    Frequently Asked Questions

    References

    1. 1.CPT® Codes and Descriptions. AAPC. Retrieved Aug 11, 2026.Maintains the CPT code set's official descriptions and guidelines, licensed from the American Medical Association, used as the definitional source for CPT codes on this page.
    2. 2.HCPCS Quarterly Update. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's quarterly release of HCPCS Level II codes and short/long descriptors, the source for HCPCS code definitions and update history.
    3. 3.ICD-10-CM Full Code List. Centers for Medicare & Medicaid Services (CMS). Retrieved Aug 11, 2026.CMS's complete ICD-10-CM diagnosis code list, used to cross-reference diagnosis codes associated with this procedure or service.
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