AutoICD API

Z84.81

Billable

Family history of carrier of genetic disease

Family history of carrier of genetic disease

Status

Billable / Specific

Block

Z77-Z99

Parent Code

Z84.8

Coding Notes

Code Also

A second code may be required; sequencing depends on circumstances

Related Codes(2)
Also Known As / Clinical Terms(47)

Clinical Terms

  • Family history of breast cancer gene BRCA mutation
  • Family history of BRCA1 gene mutation
  • Family history of breast cancer 1 gene mutation
  • Family history of genetic disease carrier
  • Family history of gene mutation
  • Family history of breast cancer 2 (BRCA2) gene mutation
  • Family history of genetic mutation for HNPCC (hereditary nonpolyposis colon cancer)
  • Family history of genetic disorder carrier
  • Family history of BRCA gene mutation
  • Family history of genetic disorder carrier (situation)
  • Family history of breast cancer 1 (BRCA1) gene mutation
  • Family history of breast cancer gene mutation in first degree relative
  • Family history of BRCA2 gene mutation
  • Family history of hereditary disease
  • Family history of hereditary disease carrier state
  • Family history of breast cancer gene (BRCA) mutation in first degree relative
  • Family history of heritable disorder
  • Family history of breast cancer 2 gene mutation
  • Family history of genetic mutation for hereditary non-polyposis colon cancer
  • Family history of genetic mutation for hereditary nonpolyposis colon cancer
  • Family history of genetic disease
  • Family history of genetic mutation for Lynch syndrome
Frequently Asked Questions
What is the ICD-10 code for family history of carrier of genetic disease?

The ICD-10-CM code for family history of carrier of genetic disease is Z84.81. The full clinical description is "Family history of carrier of genetic disease". Z84.81 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Z84.81 mean?

ICD-10-CM code Z84.81 represents “Family history of carrier of genetic disease”. 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 Z84.81 a billable code?

Yes, Z84.81 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Z84.81 in?

Z84.81 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).

What SNOMED CT codes does Z84.81 map to?

Z84.81 maps to 10 SNOMED CT concepts: 31881000119108, 431330007, 431331006, 143691000119102, 138701000119105, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Z84.81?

Z84.81 is linked to 1 UMLS Concept Unique Identifier: C2315327. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Z84.81 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like family history of carrier of genetic disease 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 Z84.81?

There is no direct ICD-11 mapping available for Z84.81 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.