Short answer · Medically reviewed summary · Last updated: 2026-04-08

Pectus excavatum is classified under the ICD-10-CM code Q67.6 (Pectus excavatum) and was previously identified under the ICD-9-CM code 754.81. These codes are essential for medical billing, insurance documentation, and clinical record-keeping for individuals navigating the complexities of this chest wall deformity. What is the clinical significance of Pectus excavatum? Pectus excavatum is a congenital chest wall deformity characterized by a concave depression of the sternum (breastbone), often referred to as "funnel chest." While it is frequently present at birth, the severity of Pectus excavatum often becomes more pronounced during the rapid growth spurts of adolescence.

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ICD10 code of Pectus excavatum and ICD9 code

ICD-10 and ICD-9 codes for Pectus excavatum, with classification details for clinicians, coders and patients.

ICD9 and ICD10 codes of Pectus excavatum

Pectus excavatum is classified under the ICD-10-CM code Q67.6 (Pectus excavatum) and was previously identified under the ICD-9-CM code 754.81. These codes are essential for medical billing, insurance documentation, and clinical record-keeping for individuals navigating the complexities of this chest wall deformity.



What is the clinical significance of Pectus excavatum?


Pectus excavatum is a congenital chest wall deformity characterized by a concave depression of the sternum (breastbone), often referred to as "funnel chest." While it is frequently present at birth, the severity of Pectus excavatum often becomes more pronounced during the rapid growth spurts of adolescence. For the 81 members of the DiseaseMaps community who live with this condition, the impact can range from mild cosmetic concerns to significant physiological challenges, such as reduced exercise tolerance or respiratory discomfort caused by the compression of the heart and lungs.



How is Pectus excavatum classified for medical records?


Accurate coding is vital for patients seeking surgical or non-surgical interventions. The transition from ICD-9 to ICD-10 allowed for more specific diagnostic tracking. The following list outlines the primary coding information for Pectus excavatum:



  • ICD-10-CM Code: Q67.6 (Congenital deformity of sternum). This is the current standard used globally for clinical documentation.

  • ICD-9-CM Code: 754.81 (Congenital musculoskeletal deformity of chest wall). This code is now largely retired but may still appear in older medical records.

  • Clinical Utility: These codes are used to justify diagnostic testing, such as chest X-rays, CT scans, or echocardiograms, which help determine the Hallers Index—a measurement used to quantify the severity of the Pectus excavatum depression.



Is Pectus excavatum hereditary or associated with other conditions?


While the exact cause of Pectus excavatum remains multifactorial, it is frequently seen in individuals with connective tissue disorders, most notably Marfan syndrome. Genetic counseling is often recommended for families where multiple members present with thoracic wall anomalies. Understanding the genetic landscape of Pectus excavatum can help clinical teams provide more personalized care plans, especially when systemic symptoms are present alongside the structural chest deformity.



What are the psychological impacts of living with Pectus excavatum?


For many, the physical appearance of Pectus excavatum can lead to significant social anxiety, body image dissatisfaction, and, in some cases, social withdrawal during the teenage years. Our clinical psychologists emphasize that the emotional burden is as valid as the physical one. Connecting with others through platforms like DiseaseMaps.org can provide a vital support system, helping individuals realize they are not alone in their journey to seeking correction or learning to manage their condition.



Next steps



  • Consult with a thoracic surgeon or a pediatric specialist if you experience shortness of breath, chest pain, or exercise intolerance.

  • Request a referral for a baseline echocardiogram or pulmonary function test to assess how the Pectus excavatum is impacting your cardiopulmonary function.

  • Join specialized patient support groups to share experiences regarding recovery from treatments like the Nuss or Ravitch procedures.

  • Track your symptoms and clinical encounters in your personal health journal to prepare for consultations with specialists.



Medical disclaimer: This information is for educational purposes only and does not constitute professional medical advice, diagnosis, or treatment; always seek the advice of your physician or other qualified health provider with any questions regarding a medical condition.



References



  • NIH Genetic and Rare Diseases Information Center (GARD): Pectus excavatum resources.

  • Orphanet: Rare disease database entry for thoracic wall malformations.

  • OMIM (Online Mendelian Inheritance in Man): Clinical synopsis for Pectus excavatum.

  • American Pediatric Surgical Association (APSA): Patient education on chest wall deformities.

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-04-08
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
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ICD9 and ICD10 codes of Pectus excavatum

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PECTUS EXCAVATUM STORIES
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Riley was born on October 28, 2005 after a fairly normal pregnancy, at home with his Dad, Grandma,and a midwife. Mom was in labor for 18 hours! When the midwife handed Riley to his mom, she noticed he had a deep indent in his chest and so she asked w...
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I have PE since I was 13 years old. Today I am 32. (Tengo PE desde los 13, hoy tengo 32 años)
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My pectus condition began to show when I was about twelve. I hated PE (or PT as it was known then) suffering ridicule from other boys. I eventually managed to be excused from games but was so ashamed of my chest that I couldn't even let my mother s...

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