The ICD-10 code for Vogt-Koyanagi-Harada Disease is H20.53. This code is used to classify and identify this specific condition in medical records and billing systems. In the previous ICD-9 coding system, the corresponding code for Vogt-Koyanagi-Harada Disease was 364.24. It is important for healthcare professionals to accurately assign these codes to ensure proper documentation and reimbursement for the treatment of this disease.
Vogt-Koyanagi-Harada (VKH) disease is a rare autoimmune condition affecting multiple systems, primarily the eyes, skin, and nervous system. It is characterized by chronic inflammation that leads to various symptoms including uveitis (inflammation of the eye), skin changes, neurological abnormalities, and auditory disturbances.
The International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for Vogt-Koyanagi-Harada disease. The ICD-10 code for VKH disease is H20.53. This code falls under the category of "Other anterior uveitis," which includes several subcategories based on the specific type and cause of uveitis. However, it is important to note that VKH disease is a complex condition that affects multiple systems, and the ICD-10 code H20.53 specifically refers to the uveitis component of VKH disease.
In contrast, the International Classification of Diseases, 9th Revision (ICD-9) did not have a specific code for Vogt-Koyanagi-Harada disease. Prior to the implementation of ICD-10, VKH disease was often coded under various general categories such as uveitis or autoimmune disorders, depending on the specific manifestations and symptoms presented by the patient.
It is worth mentioning that accurate coding of diseases is crucial for medical documentation, research, and insurance purposes. Therefore, healthcare professionals and coding specialists must stay updated with the latest coding guidelines to ensure proper identification and reporting of conditions like VKH disease.