The ICD10 code for Behcet Syndrome is M35.2. In the ICD9 coding system, Behcet Syndrome is classified under code 136.1. Behcet Syndrome is a chronic, relapsing inflammatory disorder that affects multiple systems in the body, including the skin, mucous membranes, eyes, and joints. It is characterized by recurrent oral and genital ulcers, skin lesions, and eye inflammation. Early diagnosis and treatment are crucial to manage the symptoms and prevent complications.
Behcet's syndrome, also known as Behcet's disease, is a rare autoimmune disorder characterized by recurrent oral and genital ulcers, skin lesions, and inflammation in various parts of the body. The ICD-10 code for Behcet's syndrome is M35.2. This code falls under the category of "systemic connective tissue disorders" and is used to classify and document the diagnosis of this condition in medical records.
In contrast, the ICD-9 code for Behcet's syndrome is 136.1. However, it should be noted that the ICD-9 code set has been replaced by the ICD-10 code set since October 1, 2015. The transition to ICD-10 allows for more detailed and specific coding, which aids in accurate diagnosis, treatment, and research of various medical conditions, including Behcet's syndrome.
It is important for healthcare professionals to properly document and use the correct ICD-10 code when diagnosing and treating patients with Behcet's syndrome, as it ensures accurate medical coding, billing, and statistical reporting.