ICD10 code of Paramyotonia congenita and ICD9 code

Paramyotonia congenita is a rare genetic disorder that affects the skeletal muscles, causing muscle stiffness and weakness. It is classified under the International Classification of Diseases, Tenth Revision (ICD-10) and has a specific code for identification and billing purposes.

The ICD-10 code for Paramyotonia congenita is G71.11. This code falls under the category of "Primary disorders of muscles" (G70-G73) and specifically refers to "Paramyotonia congenita" as the diagnosis. The code G71.11 helps healthcare professionals accurately identify and document cases of Paramyotonia congenita in medical records and insurance claims.

In contrast, the ICD-9 code for Paramyotonia congenita is 359.22. Under the Ninth Revision of the International Classification of Diseases (ICD-9), this code falls under the category of "Myotonia" (359) and further specifies the subtype as "Paramyotonia congenita" (359.22). The ICD-9 code system was used prior to the adoption of ICD-10.

Healthcare providers rely on these standardized codes to ensure consistency and accuracy in medical documentation, billing, and statistical analysis. These codes enable efficient communication between healthcare professionals, researchers, insurers, and policymakers, facilitating better understanding and management of various medical conditions.

It is important to note that accurate coding is crucial for reimbursement purposes, epidemiological studies, and research. Therefore, healthcare providers must assign the appropriate ICD-10 code (G71.11) or ICD-9 code (359.22) when diagnosing Paramyotonia congenita to ensure proper identification and tracking of this condition.

by Diseasemaps