ICD10 code of Hereditary multiple exostoses and ICD9 code

Hereditary multiple exostoses (HME) is a rare genetic disorder characterized by the development of multiple benign bone tumors called exostoses. These exostoses typically occur near the growth plates of long bones, such as the femur, tibia, and humerus. HME is an autosomal dominant condition, meaning that it can be passed down from one generation to the next.

In the International Classification of Diseases, 10th Revision (ICD-10), the specific code for Hereditary multiple exostoses is Q78.1. This code falls under the broader category of "Other osteochondrodysplasia with defects of growth of tubular bones and spine." It helps healthcare professionals accurately identify and classify this particular disorder when making diagnoses or conducting research.

On the other hand, in the previous edition, the International Classification of Diseases, 9th Revision (ICD-9), Hereditary multiple exostoses is classified under code 756.59. This code falls under the category of "Other congenital musculoskeletal anomalies." However, it is essential to note that the transition from ICD-9 to ICD-10 occurred in October 2015, and the latter is now the standard coding system used worldwide.

By using these specific ICD codes, healthcare providers can accurately document and track the occurrence of Hereditary multiple exostoses. This information is crucial for research purposes, monitoring disease prevalence, and ensuring appropriate medical care and management for affected individuals.

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by Diseasemaps