myICD10.com Logo
complete trisomy 13 syndrome

Medical Definition

A syndrome characterized by the presence of three complete copies of genetic material for chromosome 13, instead of the normal two. it leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities.
Related Codes (1)
Code
Description
Billable
Details
Q91.7Trisomy 13, unspecified

Rows per page

Page 1 of 1