Z13.7 - Encounter for screening for genetic and chromosomal anomalies

The ICD 10 Code for Encounter for screening for genetic and chromosomal anomalies is listed as Z13.7.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field	Value
Diagnosis Code:	Z13.7
Description:	Encounter for screening for genetic and chromosomal anomalies Excludes1: genetic testing for procreative management (Z31.4-)

Chapter	Factors influencing health status and contact with health services (Z00-Z99)
Block	Persons encountering health services for examinations (Z00-Z13)
Parent	Z13 - Encounter for screening for other diseases and disorders
ICD-10-CM Children (deeper level / typically more specific) of Z13.7:
Z13.71 - Encounter for nonprocreative screening for genetic disease carrier status
Z13.79 - Encounter for other screening for genetic and chromosomal anomalies
ICD-10-CM Siblings (same level / similar specificity) of Z13.7:
Z13.0 - Encounter for screening for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Z13.1 - Encounter for screening for diabetes mellitus
Z13.2 - Encounter for screening for nutritional, metabolic and other endocrine disorders
Z13.4 - Encounter for screening for certain developmental disorders in childhood
Z13.5 - Encounter for screening for eye and ear disorders
Z13.6 - Encounter for screening for cardiovascular disorders
Z13.8 - Encounter for screening for other specified diseases and disorders
Z13.9 - Encounter for screening, unspecified