ICD10 code of Central Core Disease and ICD9 code

Central core disease (CCD) is a rare genetic neuromuscular disorder that primarily affects skeletal muscles. It is characterized by muscle weakness, hypotonia (reduced muscle tone), delayed motor development, and potential skeletal abnormalities. Although CCD is typically inherited in an autosomal dominant pattern, sporadic cases can also occur.

In the International Classification of Diseases, 10th Revision (ICD-10), the specific code for Central Core Disease is G71.2. This code falls under the broader category of "Congenital Myopathies," which encompasses various inherited muscle disorders. The code G71.2 is used to identify CCD in medical records, insurance claims, and statistical data.

On the other hand, in the previous version, the International Classification of Diseases, 9th Revision (ICD-9), Central Core Disease was classified under the code 359.0. This code was used to denote "Congenital Myopathies" in general, without specific differentiation between different subtypes.

It is important to note that the transition from ICD-9 to ICD-10 occurred on October 1, 2015, so healthcare providers and systems now primarily use the ICD-10 coding system for accurate diagnosis and reporting of medical conditions. The ICD-10 codes provide greater specificity and allow for better tracking and analysis of diseases and their associated treatments.

In summary, the ICD-10 code for Central Core Disease is G71.2, while the corresponding ICD-9 code was 359.0. These codes assist in the standardized classification and documentation of CCD, facilitating accurate diagnosis, treatment, and research on this rare neuromuscular disorder.

by Diseasemaps