Z13.79
BillableEncntr for oth screening for genetic and chromsoml anomalies
Encounter for other screening for genetic and chromosomal anomalies
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 managementZ31.4
Also Known As / Clinical Terms(10)
SNOMED CT
UMLS
Clinical Terms
- Down screening - blood sent
- Down screening status
- Down's screening status
- Down's screening - blood sent
Frequently Asked Questions
What is the ICD-10 code for encntr for oth screening for genetic and chromsoml anomalies?
The ICD-10-CM code for encntr for oth screening for genetic and chromsoml anomalies is Z13.79. The full clinical description is "Encounter for other screening for genetic and chromosomal anomalies". Z13.79 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z13.79 mean?
ICD-10-CM code Z13.79 represents “Encounter for other screening for genetic and chromosomal anomalies”. It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a billable/specific code that can be used on a claim.
Is Z13.79 a billable code?
Yes, Z13.79 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z13.79 in?
Z13.79 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What codes cannot be used with Z13.79?
Z13.79 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 SNOMED CT codes does Z13.79 map to?
Z13.79 maps to 2 SNOMED CT concepts: 169797001, 243832003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z13.79?
Z13.79 is linked to 1 UMLS Concept Unique Identifier: C2910623. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Z13.79 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like encntr for oth screening for genetic and chromsoml 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.
What is the ICD-11 equivalent of Z13.79?
There is no direct ICD-11 mapping available for Z13.79 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.