ICD10 code of Friedreich Ataxia and ICD9 code

Friedreich Ataxia is a rare genetic disorder characterized by progressive damage to the nervous system, leading to muscle weakness, impaired coordination, and other debilitating symptoms. In the International Classification of Diseases, 10th Revision (ICD-10), the code for Friedreich Ataxia is G11.1. This code falls under the category of "Hereditary ataxia."

In the previous version, the International Classification of Diseases, 9th Revision (ICD-9), the code for Friedreich Ataxia was 334.1. This code was categorized under "Spinocerebellar degenerations."

It is important to note that ICD codes are used for medical billing, statistical tracking, and research purposes. They provide a standardized way of categorizing and identifying various diseases and conditions. These codes aid in accurate documentation and communication among healthcare professionals, insurance providers, and researchers.

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by Diseasemaps