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    v1.0.28
    OpenPayerBilling CodesOther congenital malformations of the digestive systemICD-10-CM q43-other-congenital-malformations-of-intestine
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    ICD-10-CM Code For Other Congenital Malformations Of Intestine: Group Overview

    The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group Q43 includes congenital malformations of the intestine such as intestinal atresia, stenosis, duplications, and other developmental anomalies affecting intestinal structure and function. These ICD-10-CM diagnosis codes are used to document patients with congenital intestinal defects, capturing anatomic location, presence of obstruction or perforation, and associated clinical complexity. Accurate coding within the ICD-10-CM Q43 group supports proper claim adjudication, complete clinical documentation, and appropriate reimbursement.

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    ICD-10-CM Q43: Other Congenital Malformations Of Intestine Overview

    This group includes congenital structural anomalies of the intestine present at birth that affect intestinal form and function. It targets congenital malformations of the digestive system, specifically intestinal atresia, stenosis, and other developmental anomalies. Accurate coding matters for clinical records, appropriate classification of congenital conditions, and reimbursement support tied to documented complexity.

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    When to Use

    Use a code from this group when documenting a congenital intestinal malformation identified clinically, radiographically, or surgically in a patient. Select the most specific code that indicates the type and location of the intestinal anomaly and any associated complications.

    ICD-10-CM Codes

    10 rows

    ICD-10-CM CodeDescription
    Q43.0Meckel's diverticulum (displaced) (hypertrophic)
    Q43.1Hirschsprung's disease
    Q43.2Other congenital functional disorders of colon
    Q43.3Congenital malformations of intestinal fixation
    Q43.4Duplication of intestine
    Q43.5Ectopic anus
    Q43.6Congenital fistula of rectum and anus
    Q43.7Persistent cloaca
    Q43.8Other specified congenital malformations of intestine
    Q43.9Congenital malformation of intestine, unspecified

    DRG Codes

    6 rows

    DRG CodeDescription
    380Complicated Peptic Ulcer with MCC
    381Complicated Peptic Ulcer with CC
    382Complicated Peptic Ulcer without CC/MCC
    393Other Digestive System Diagnoses with MCC
    394Other Digestive System Diagnoses with CC
    395Other Digestive System Diagnoses without CC/MCC

    Typical Clinical Scenarios

    • A neonate presents in the first days of life with bilious vomiting, abdominal distension, and failure to pass meconium; abdominal radiographs suggest distal intestinal obstruction and contrast enema indicates colonic atresia. The infant undergoes surgical exploration confirming an atretic segment of the colon requiring resection and primary anastomosis; a congenital malformation of the intestine is assigned to capture the anatomical defect. Typical codes: Q43.2, Q43.3
    • A young child has chronic intermittent abdominal pain, poor weight gain, and episodes of constipation since infancy; imaging and endoscopic evaluation identify congenital malrotation with associated nonobstructive intrinsic narrowing of a segment of small intestine causing dysmotility symptoms. The chronic structural anomaly of the intestine is coded to reflect the congenital cause of the ongoing digestive symptoms and growth issues. Typical codes: Q43.1, Q43.4
    • An adult with a history of repaired congenital intestinal atresia in childhood presents with acute small bowel obstruction from adhesive stricturing at the surgical anastomosis, with nausea, vomiting, and obstipation requiring admission and possible surgical intervention. The encounter documents a complication related to a prior congenital intestinal malformation and its repair, so a code for the congenital malformation of the intestine is used alongside acute management codes. Typical codes: Q43.5, Q43.9}

    Related Codes

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

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

    Q39-CONGENITAL-MALFORMATIONS-OF-ESOPHAGUS

    ICD-10-CM Code For Congenital Malformations Of Esophagus: 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

    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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