myICD10.com Logo
prader–willi syndrome

Wikipedia Summary

Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In newborns, symptoms include weak muscles, poor feeding, and slow development...
Related Codes (1)
Code
Description
Billable
Details
Q87.11Prader-Willi syndrome

Rows per page

Page 1 of 1