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

Jackson-Weiss Syndrome, also known as JWS, is a rare genetic disorder characterized by craniosynostosis (premature fusion of skull bones) and foot abnormalities. While I am not a medical professional, I can provide some information on the coding for this syndrome.

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ICD10 code of Jackson-Weiss Syndrome and ICD9 code

ICD-10 and ICD-9 codes for Jackson-Weiss Syndrome, with classification details for clinicians, coders and patients.

ICD9 and ICD10 codes of Jackson-Weiss Syndrome
Jackson-Weiss Syndrome, also known as JWS, is a rare genetic disorder characterized by craniosynostosis (premature fusion of skull bones) and foot abnormalities. While I am not a medical professional, I can provide some information on the coding for this syndrome. In the International Classification of Diseases, Tenth Revision (ICD-10), the code for Jackson-Weiss Syndrome is Q87.1. This code falls under the category of "Congenital malformation syndromes predominantly associated with short stature," which encompasses various genetic conditions with skeletal abnormalities.

On the other hand, in the previous version of the classification system, the ICD-9 code for Jackson-Weiss Syndrome is 756.0. Under ICD-9, this code falls under the broader category of "Anomalies of the skull and face bones." It is important to note that the ICD-9 code system was replaced by ICD-10 in October 2015 to provide a more detailed and comprehensive classification of diseases and disorders.

It is always advisable to consult with a qualified healthcare professional or medical coder for accurate and up-to-date coding information.
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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