ICD10 code of Galactosemia and ICD9 code

Galactosemia is a rare genetic disorder that affects the body's ability to metabolize galactose, a sugar found in milk and dairy products. It is caused by a deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT), leading to an accumulation of galactose and its byproducts in the body. This condition can result in severe complications if not properly managed.

In the International Classification of Diseases, 10th Revision (ICD-10), the specific code for galactosemia is E74.21. This code falls under the broader category of "Disorders of galactose metabolism." The ICD-10 code system is used worldwide to classify and code various diseases, disorders, and health conditions, enabling healthcare professionals to accurately document and track patient diagnoses.

In the previous version of the classification system, the ICD-9 code for galactosemia was 271.1. The transition from ICD-9 to ICD-10 allowed for greater specificity and detail in diagnosing and coding medical conditions, providing a more comprehensive understanding of the patient's condition.

It is crucial for healthcare providers to correctly assign the appropriate ICD-10 code for galactosemia to ensure accurate documentation, effective treatment, and appropriate reimbursement. By using standardized codes, healthcare professionals, researchers, and policymakers can analyze data, monitor trends, and improve the overall management and understanding of galactosemia.

by Diseasemaps