Z13.7

The ICD-10-CM code for encntr screen for genetic and chromosomal anomalies is Z13.7. The full clinical description is "Encounter for screening for genetic and chromosomal anomalies". Z13.7 is a non-billable header code. Use a more specific child code for billing purposes.

ICD-10-CM code Z13.7 represents “Encounter for screening for genetic and chromosomal anomalies”. It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a non-billable header code. Use a more specific child code for billing purposes.

No, Z13.7 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 2 child codes under Z13.7.

Z13.7 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).

Z13.7 has Excludes1 notes indicating codes that cannot be used together with it, including: examinations related to pregnancy and reproduction (Z30-Z36, Z39.-); encounter for diagnostic examination-code to sign or symptom; genetic testing for procreative management (Z31.4-).

Z13.7 has 2 child codes, including: Z13.71 (Encntr for nonprocreat screen for genetic dis carrier status), Z13.79 (Encntr for oth screening for genetic and chromsoml anomalies).

Z13.7 is linked to 1 UMLS Concept Unique Identifier: C2910621. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like encntr screen for genetic and chromosomal anomalies affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

Z13.7 maps to the ICD-11 code: QA0A.Y (Special screening for diseases or disorders, not elsewhere classified).