ICD10 code of Dysferlinopathy - Miyoshi Myopathy and ICD9 code

Dysferlinopathy, specifically Miyoshi Myopathy, is a rare genetic disorder characterized by progressive muscle weakness and wasting primarily affecting the distal muscles of the lower limbs. This condition falls under the broader category of muscular dystrophies and is caused by mutations in the dysferlin gene.

In terms of medical coding, the International Classification of Diseases, 10th Revision (ICD-10), provides a specific code for Dysferlinopathy - Miyoshi Myopathy. The appropriate code for this condition is G71.0. This code is used to classify various muscular dystrophies, including Miyoshi Myopathy, in the ICD-10 system.

On the other hand, in the previous ICD-9 system, there was not a specific code for Dysferlinopathy - Miyoshi Myopathy. Under ICD-9, muscular dystrophies were classified under a broader code category, such as 359.1, which encompassed various types of muscular dystrophies.

It is important to note that medical coding is a complex and evolving field, and there may be updates or changes in coding systems over time. Therefore, it is always recommended to consult the most recent coding guidelines and resources for accurate and up-to-date information on specific codes.

In conclusion, the ICD-10 code for Dysferlinopathy - Miyoshi Myopathy is G71.0, while the ICD-9 code for this specific condition was not available, and broader codes for muscular dystrophies were used.