Léri-Weill dyschondrosteosis is a rare genetic disorder that affects bone development, specifically the growth plates in the arms and legs. It is characterized by short stature, short forearms and lower legs, and a characteristic deformity of the wrist called Madelung deformity. This condition primarily affects females, with symptoms typically appearing during childhood or adolescence.
In terms of medical coding, Léri-Weill dyschondrosteosis is classified under the International Classification of Diseases, 10th Revision (ICD-10). The specific ICD-10 code for this condition is Q77.4. This code falls under the category of "Other osteochondrodysplasia with defects of growth of tubular bones and spine," which encompasses various skeletal dysplasias involving growth plate abnormalities.
On the other hand, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10. However, for reference purposes, the corresponding ICD-9 code for Léri-Weill dyschondrosteosis is 756.4. This code falls under the category of "Other congenital musculoskeletal deformities," which includes various other skeletal abnormalities.
It's important to note that accurate coding is crucial for medical records, billing, and research purposes. These codes help healthcare professionals and researchers classify and track different conditions, allowing for better understanding, treatment, and monitoring of various diseases and disorders.
In conclusion, the ICD-10 code for Léri-Weill dyschondrosteosis is Q77.4, while the corresponding ICD-9 code is 756.4. These codes are essential for accurate documentation and classification of the condition in medical practice.
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.