Short answer · Medically reviewed summary · Last updated: 2023-07-10

Pycnodysostosis is a rare genetic disorder characterized by abnormal bone development and increased bone density. The condition is also known as Toulouse-Lautrec syndrome, after the famous French painter who is believed to have had this condition. In terms of medical coding, Pycnodysostosis is classified under the International Classification of Diseases, 10th Revision (ICD-10).

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ICD10 code of Pycnodysostosis and ICD9 code

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

ICD9 and ICD10 codes of Pycnodysostosis
Pycnodysostosis is a rare genetic disorder characterized by abnormal bone development and increased bone density. The condition is also known as Toulouse-Lautrec syndrome, after the famous French painter who is believed to have had this condition.

In terms of medical coding, Pycnodysostosis is classified under the International Classification of Diseases, 10th Revision (ICD-10). The specific ICD-10 code for Pycnodysostosis is Q78.8. This code falls under the category of "Other specified osteochondrodysplasias," which includes various skeletal disorders with similar features.

On the other hand, the International Classification of Diseases, 9th Revision (ICD-9) code for Pycnodysostosis is 756.59. In the ICD-9 system, this code is found under the classification of "Other congenital musculoskeletal anomalies." It is important to note that the ICD-9 system has been replaced by the ICD-10 system in most countries, as it provides more specific and detailed codes for various conditions.

Medical coding using ICD-10 and ICD-9 is crucial for healthcare professionals and insurance providers to accurately document and categorize patients' diagnoses and treatments. These codes help in streamlining medical records, facilitating communication among healthcare providers, and enabling proper reimbursement for services.

In conclusion, the ICD-10 code for Pycnodysostosis is Q78.8, and the corresponding ICD-9 code is 756.59. These codes assist in organizing and classifying medical information, ensuring effective healthcare management for individuals with this rare genetic disorder.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
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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