Z13.7

Non-billable

Encntr screen for genetic and chromosomal anomalies

Encounter for screening for genetic and chromosomal anomalies

This is a header/category code. For billing purposes, use a more specific child code from the list below.

Status

Non-billable / Header

Block

Z00-Z13

Parent Code

Z13

Child Codes

2

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

  • 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-)

Child Codes (2)

Also Known As / Clinical Terms

Frequently Asked Questions

What is the ICD-10 code for encntr screen for genetic and chromosomal anomalies?

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.

What does ICD-10 code Z13.7 mean?

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.

Is Z13.7 a billable code?

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.

What chapter is Z13.7 in?

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

What codes cannot be used with Z13.7?

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-).

What are the subcategories under Z13.7?

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).

What are the UMLS CUIs for Z13.7?

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.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.