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    v1.0.28
    OpenPayerBilling CodesOther congenital malformations of the digestive systemICD-10-CM q39-congenital-malformations-of-esophagus
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    ICD-10-CM Code For Congenital Malformations Of Esophagus: Group Overview

    The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group Q39 includes congenital anomalies of the esophagus such as esophageal atresia and tracheoesophageal fistula that impair continuity or connection of the esophagus. These ICD-10-CM diagnosis codes are used to document newborn and pediatric presentations with feeding intolerance, aspiration risk, respiratory complications, and related surgical repairs. Accurate coding within the ICD-10-CM Q39 group supports proper claim adjudication and complete clinical documentation for appropriate reimbursement.

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    ICD-10-CM Q39: Congenital Malformations Of Esophagus Overview

    This group includes congenital anomalies of the esophagus such as atresia and tracheoesophageal fistula that affect swallowing and airway protection. These diagnoses target the upper gastrointestinal tract and are typically identified in neonates or infants with feeding difficulties or respiratory compromise. Accurate coding matters for appropriate clinical documentation and reimbursement because it reflects congenital severity, required interventions, and resource use.

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    When to Use

    Use a code from this group when a congenital esophageal anomaly has been diagnosed, documented, or treated, such as during neonatal admission for feeding difficulty or surgical repair. Select the specific code that reflects the exact anatomical defect and any associated features documented by the clinician.

    ICD-10-CM Codes

    9 rows

    ICD-10-CM CodeDescription
    Q39.0Atresia of esophagus without fistula
    Q39.1Atresia of esophagus with tracheo-esophageal fistula
    Q39.2Congenital tracheo-esophageal fistula without atresia
    Q39.3Congenital stenosis and stricture of esophagus
    Q39.4Esophageal web
    Q39.5Congenital dilatation of esophagus
    Q39.6Congenital diverticulum of esophagus
    Q39.8Other congenital malformations of esophagus
    Q39.9Congenital malformation of esophagus, unspecified

    DRG Codes

    3 rows

    DRG CodeDescription
    368Major Esophageal Disorders with MCC
    369Major Esophageal Disorders with CC
    370Major Esophageal Disorders without CC/MCC

    Typical Clinical Scenarios

    • A neonate is born with excessive oral secretions, choking on feeds and cyanotic spells during attempts at feeding; contrast esophagram in the newborn nursery demonstrates a blind-ending proximal esophageal pouch with a tracheoesophageal fistula. Surgical repair is planned during the infant’s initial hospitalization, and a congenital malformation of the esophagus diagnosis is assigned to document the anatomical anomaly causing feeding compromise. Typical codes: Q39.1, Q39.2
    • A toddler with a history of recurrent aspiration pneumonia and chronic cough is evaluated by pediatric gastroenterology and otolaryngology; endoscopic assessment reveals an esophageal atresia previously undiagnosed with an abnormal communication to the airway identified. The chronic respiratory and feeding symptoms prompt coding of the congenital esophageal malformation as the underlying cause of the recurrent pulmonary disease. Typical codes: Q39.1, Q39.3
    • An adult presents for preoperative assessment after longstanding dysphagia and prior childhood repair of an esophageal congenital anomaly; imaging and endoscopy demonstrate stricturing and dysmotility at the repair site requiring dilation and nutritional support. A congenital malformation-related diagnosis is assigned to capture the repaired congenital abnormality as the source of current complications and to guide perioperative management. Typical codes: Q39.4, Q39.6

    Related Codes

    Q38-OTHER-CONGENITAL-MALFORMATIONS-TONGUE-MOUTH-PHARYNX

    ICD-10-CM Code For Other Congenital Malformations Of Tongue Mouth And Pharynx: Group Overview

    Q40-OTHER-CONGENITAL-MALFORMATIONS-UPPER-ALIMENTARY-TRACT

    ICD-10-CM Code For Other Congenital Malformations Of Upper Alimentary Tract: Group Overview

    Q41-CONGENITAL-ABSENCE-ATRESIA-STENOSIS-SMALL-INTESTINE

    ICD-10-CM Code For Congenital Absence, Atresia And Stenosis Of Small Intestine: Group Overview

    Q42-CONGENITAL-LARGE-INTESTINE-MALFORMATIONS

    ICD-10-CM Code For Congenital Absence, Atresia And Stenosis Of Large Intestine: Group Overview

    Q43-OTHER-CONGENITAL-MALFORMATIONS-OF-INTESTINE

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

    Q44-CONGENITAL-MALFORMATIONS-OF-GALLBLADDER

    ICD-10-CM Code For Congenital Malformations Of Gallbladder, Bile Ducts And Liver: Group Overview

    Q45-OTHER-CONGENITAL-MALFORMATIONS-DIGESTIVE

    ICD-10-CM Code For Other Congenital Malformations Of Digestive 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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