ICD10 code of 48,XXYY syndrome and ICD9 code

48,XXYY syndrome is a rare genetic disorder that affects males. In this condition, individuals have an extra copy of both the X and Y chromosomes, resulting in a total of 48 chromosomes instead of the typical 46. This genetic anomaly leads to various physical, cognitive, and developmental challenges.

In terms of medical coding, the International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for 48,XXYY syndrome. The appropriate ICD-10 code for this condition is Q98.8. This code falls under the category of "Other specified congenital malformations of the chromosome," which encompasses unique chromosomal disorders that are not covered by other specific codes.

Regarding the ICD-9 code, it is essential to note that the ICD-10 coding system replaced ICD-9 in 2015. Therefore, ICD-9 does not have a dedicated code for 48,XXYY syndrome. However, in ICD-9, similar conditions such as Klinefelter syndrome (47,XXY) and other chromosomal abnormalities may have specific codes.

It is crucial to consult with a healthcare professional or medical coding specialist for accurate and up-to-date coding information, as they can provide specific guidance based on the latest coding guidelines and conventions.

by Diseasemaps