The ICD-10 code for Leri Pleonosteosis is Q78.8. This code is used to classify this rare genetic disorder characterized by skeletal abnormalities. Unfortunately, there is no specific ICD-9 code for Leri Pleonosteosis as it was replaced by the ICD-10 coding system. It is important to consult with a healthcare professional for accurate diagnosis and coding information.
Leri Pleonosteosis, also known as Leri Weill Dyschondrosteosis, is a rare genetic disorder that affects the development of bones. It is characterized by short stature, abnormal curvature of the forearm bones, and shortening of the lower legs.
In terms of medical coding, Leri Pleonosteosis is classified under the International Classification of Diseases, Tenth Revision (ICD-10). The specific ICD-10 code for Leri Pleonosteosis is Q78.8. This code falls under the category of "Other specified osteochondrodysplasias," which includes various rare skeletal disorders with distinct features.
As for the previous version of the coding system, the International Classification of Diseases, Ninth Revision (ICD-9), the corresponding code for Leri Pleonosteosis is 756.4. In ICD-9, this condition is classified under "Other congenital musculoskeletal anomalies." However, it is essential to note that the ICD-9 codes have been replaced by ICD-10 codes since October 1, 2015, as ICD-10 provides more detailed and specific codes for various medical conditions.
It is important to consult with a healthcare professional or medical coder for accurate coding and billing purposes. They will be able to provide the most up-to-date information regarding medical coding and ensure proper reimbursement for medical services related to Leri Pleonosteosis.