Juvenile polyposis syndrome is a rare genetic disorder characterized by the development of multiple polyps in the gastrointestinal tract. The ICD-10 code for this condition is K63.5. Unfortunately, there is no specific ICD-9 code for juvenile polyposis syndrome as it has been replaced by the newer coding system. It is important to consult with a healthcare professional for accurate diagnosis and coding.
Juvenile polyposis syndrome (JPS) is a rare genetic disorder characterized by the presence of multiple polyps in the gastrointestinal tract. These polyps predominantly occur in the colon, but can also be found in the stomach and small intestine. Due to its genetic nature, JPS often presents during childhood or adolescence.
In the International Classification of Diseases, Tenth Revision (ICD-10), the specific code for Juvenile polyposis syndrome is K63.5. This code falls under the chapter "Diseases of the digestive system" and specifically refers to "Polyp of colon." While the ICD-10 code provides a standardized way to classify and identify this condition, it is important to note that medical professionals may also use additional codes to further specify the location or extent of the polyps.
In the previous edition, the ninth revision (ICD-9), Juvenile polyposis syndrome was classified under code 569.0, which encompassed "Other disorders of intestine." However, it is important to transition to the more current ICD-10 coding system, as it offers a more detailed and comprehensive classification of diseases.
It is crucial to consult with a healthcare professional or certified medical coder for accurate coding and diagnosis. These codes assist in medical record keeping, insurance reimbursement, and statistical analysis, ultimately aiding in research and improving patient care.