Turcot Syndrome is a rare genetic disorder characterized by the development of colorectal cancer and brain tumors. The ICD-10 code for Turcot Syndrome is Q85.8, which falls under the category of "Other phakomatoses, not elsewhere classified." Unfortunately, there is no specific ICD-9 code for Turcot Syndrome as it has been replaced by the newer ICD-10 coding system.
Turcot Syndrome is a rare genetic disorder characterized by the occurrence of both colorectal cancer and brain tumors, specifically glioblastoma. The International Classification of Diseases, 10th Revision (ICD-10), provides a specific code for this condition. The ICD-10 code for Turcot Syndrome is Q85.8. This code falls under the category of "Other phakomatoses, not elsewhere classified." It is important to note that the ICD-10 code is used internationally for medical coding and billing purposes.
In contrast, the International Classification of Diseases, 9th Revision (ICD-9), which was used prior to the implementation of ICD-10, provided a different coding system. The ICD-9 code for Turcot Syndrome is 759.6. This code falls under the category of "Other congenital anomalies of intestine." However, it is crucial to remember that ICD-9 codes are outdated and no longer used for medical coding and billing purposes.
It is always recommended to consult with a healthcare professional or medical coder for accurate and up-to-date coding information.