Juvenile Hemochromatosis is a rare genetic disorder characterized by excessive iron accumulation in the body, leading to organ damage. The ICD-10 code for Juvenile Hemochromatosis is E83.110. Unfortunately, there is no specific ICD-9 code for Juvenile Hemochromatosis as it was replaced by ICD-10. Proper diagnosis and management are crucial to prevent complications associated with iron overload.
Juvenile Hemochromatosis is a rare genetic disorder characterized by excessive iron accumulation in various organs of the body, leading to organ damage and dysfunction. The International Classification of Diseases, 10th Revision (ICD-10) provides a specific code to identify this condition. The ICD-10 code for Juvenile Hemochromatosis is E83.110.
In contrast, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10. However, for reference purposes, the corresponding ICD-9 code for Juvenile Hemochromatosis is 275.01.
It is important to note that the transition from ICD-9 to ICD-10 occurred on October 1, 2015, and healthcare providers and institutions are now required to use ICD-10 codes for billing, documentation, and statistical purposes. The updated coding system provides more specific and detailed codes, allowing for better characterization and classification of diseases and conditions.
Juvenile Hemochromatosis typically manifests in individuals during adolescence or early adulthood and presents with symptoms such as fatigue, weakness, joint pain, and abdominal pain. If left untreated, it can lead to severe complications including liver cirrhosis, heart failure, and endocrine dysfunction.
In conclusion, the ICD-10 code for Juvenile Hemochromatosis is E83.110, while the corresponding ICD-9 code is 275.01. These codes are used to accurately identify and classify this rare genetic disorder in medical records, facilitating appropriate treatment and management for affected individuals.