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    OpenPayerBilling CodesCongenital malformations of the urinary systemICD-10-CM q64-other-congenital-malformations-of-urinary-system
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    ICD-10-CM Code For Other Congenital Malformations Of Urinary System: Group Overview

    The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group Q64 includes congenital malformations of the urinary system such as renal hypoplasia, renal dysplasia, ectopic kidney, duplication anomalies, and other specified congenital anomalies of the kidneys, ureters, and bladder. These ICD-10-CM diagnosis codes are used to document congenital structural abnormalities of urinary organs, capturing anatomic details, laterality, and any associated functional impairment important for clinical records. Accurate coding within the ICD-10-CM Q64 group supports proper claim adjudication, complete clinical documentation, and appropriate reimbursement.

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    ICD-10-CM Q64: Other Congenital Malformations Of Urinary System Overview

    The ICD-10-CM Q64 code group covers congenital structural anomalies of the urinary tract that are not classified elsewhere. These diagnoses target malformations of kidneys, ureters, bladder, and related urinary structures present at birth. Accurate coding supports appropriate claim processing and reflects clinical complexity relevant to care and resource use.

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    When to Use

    Assign a code from this group when a congenital structural anomaly of the urinary tract is the documented diagnosis and pertains to clinical care, evaluation, or billing. Use the most specific code available to reflect the anatomic site, laterality, and any noted functional impairment.

    ICD-10-CM Codes

    22 rows

    ICD-10-CM CodeDescription
    Q64.0Epispadias
    Q64.10Exstrophy of urinary bladder, unspecified
    Q64.11Supravesical fissure of urinary bladder
    Q64.12Cloacal exstrophy of urinary bladder
    Q64.19Other exstrophy of urinary bladder
    Q64.2Congenital posterior urethral valves
    Q64.31Congenital bladder neck obstruction
    Q64.32Congenital stricture of urethra
    Q64.33Congenital stricture of urinary meatus
    Q64.39Other atresia and stenosis of urethra and bladder neck
    Q64.4Malformation of urachus
    Q64.5Congenital absence of bladder and urethra
    Q64.6Congenital diverticulum of bladder
    Q64.70Unspecified congenital malformation of bladder and urethra
    Q64.71Congenital prolapse of urethra
    Q64.72Congenital prolapse of urinary meatus
    Q64.73Congenital urethrorectal fistula
    Q64.74Double urethra
    Q64.75Double urinary meatus
    Q64.79Other congenital malformations of bladder and urethra

    Showing 1–20 of 22

    DRG Codes

    5 rows

    DRG CodeDescription
    698Other Kidney and Urinary Tract Diagnoses with MCC
    699Other Kidney and Urinary Tract Diagnoses with CC
    700Other Kidney and Urinary Tract Diagnoses without CC/MCC
    729Other Male Reproductive System Diagnoses with CC/MCC
    730Other Male Reproductive System Diagnoses without CC/MCC

    Typical Clinical Scenarios

    • A newborn male is noted on newborn exam and prenatal ultrasound to have an abdominal mass and poor urine output; postnatal ultrasound demonstrates hydronephrosis and a unilateral duplicated renal pelvis with duplex collecting system leading to recurrent urinary stasis. The infant is referred to pediatric urology for evaluation of obstruction and possible surgical correction; a congenital anomaly of the renal collecting system is assigned to describe the structural duplication. Typical codes: Q64.31, Q64.32, Q64.33
    • A school-age child with a history of recurrent urinary tract infections and daytime urinary incontinence undergoes voiding cystourethrogram and renal ultrasound showing vesicoureteral reflux associated with congenital posterior urethral valves and bladder diverticulum. The child presents for outpatient evaluation and long-term management of the anatomic cause of recurrent infections and bladder dysfunction; a congenital malformation of the bladder outlet or urethra is coded to capture the underlying congenital abnormality. Typical codes: Q64.10, Q64.11, Q64.12
    • An adult presents to the emergency department with acute flank pain and sepsis from obstructive pyelonephritis; imaging reveals a single ectopic kidney with severe hydronephrosis and stone formation causing urinary obstruction. The congenital positional anomaly of the kidney is documented as the underlying condition contributing to the acute complication and guides both acute management and future urologic planning. Typical codes: Q64.4, Q64.5

    Related Codes

    Q60-RENAL-AGENESIS-AND-REDUCTION-DEFECTS

    ICD-10-CM Code For Renal Agenesis And Other Reduction Defects Of Kidney: Group Overview

    Q61-CYSTIC-KIDNEY-DISEASE

    ICD-10-CM Code For Cystic Kidney Disease: Group Overview

    Q62-CONGENITAL-OBSTRUCTIVE-DEFECTS-RENAL-PELVIS-URETER

    ICD-10-CM Code For Congenital Obstructive Defects Of Renal Pelvis And Congenital Malformations Of Ureter: Group Overview

    Q63-OTHER-CONGENITAL-MALFORMATIONS-OF-KIDNEY

    ICD-10-CM Code For Other Congenital Malformations Of Kidney: 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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