Z15.89

Billable

Genetic susceptibility to other disease

Genetic susceptibility to other disease

Status

Billable / Specific

Block

Z14-Z15

Parent Code

Z15.8

Coding Notes

Includes

Conditions included under this code

  • confirmed abnormal gene

Excludes 1

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

Use Additional Code

Additional codes that should follow this code

Related Codes(1)
Z15.81

Genetic susceptibility to multiple endocrine neoplasia [MEN]

Billable
Also Known As / Clinical Terms(121)

SNOMED CT

UMLS

Clinical Terms

  • Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation
  • Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
  • Genetic susceptibility to genetic disorder
  • Uncertain genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial IRF8 (interferon regulatory factor 8) deficiency
  • Autosomal recessive MSMD (mendelian susceptibility to mycobacterial disease) due to complete RORgamma receptor mutation
  • Genetic susceptibility to malignant hyperthermia due to RYR1 (ryanodine receptor 1) gene mutation positive
  • Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR1 deficiency
  • Susceptibility to infection due to TYK2 deficiency
  • Mendelian susceptibility to mycobacterial disease
  • Susceptibility to infection due to tyrosine kinase 2 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency
  • Predisposition to severe viral infection due to IRF7 deficiency
  • Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation
  • Mendelian susceptibility to mycobacterial disease due to partial STAT1 (signal transducer and activator of transcription 1) deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
  • Mendelian susceptibility to mycobacterial infection
  • Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR2 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete IL12B deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
  • Storage pool deficiency
  • Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation
  • Uncertain genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation
  • Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation
  • Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency
  • Malignant hyperthermia genetic susceptibility
  • Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation
  • Predisposition to severe viral infection due to interferon regulatory factor 7 deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
  • Predisposition to invasive fungal disease due to CARD9 deficiency
  • Genetic susceptibility to cardiovascular disorder
  • MSMD - mendelian susceptibility to mycobacterial disease
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
  • Dense body defect
  • Autosomal recessive primary immunodeficiency due to RORC mutation
  • Autosomal recessive hyper-IgE (immunoglobulin E) syndrome due to TYK2 deficiency
  • Familial platelet syndrome with predisposition to acute myelogenous leukemia
  • Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
  • Malignant hyperthermia predisposition due to CACNA1S (calcium voltage-gated channel subunit alpha1 S) gene mutation positive
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency
  • Familial platelet disorder with associated myeloid malignancy
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial janus kinase 1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete ISG15 (interferon stimulated gene 15) deficiency
  • Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation positive
  • Familial platelet syndrome with predisposition to acute myelogenous leukaemia
  • Genetic susceptibility to malignant hyperthermia
  • Invasive candidiasis, deep dermatophytosis syndrome
  • Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation positive
  • X-linked mendelian susceptibility to mycobacterial disease
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation
  • Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency
Frequently Asked Questions
What is the ICD-10 code for genetic susceptibility to other disease?

The ICD-10-CM code for genetic susceptibility to other disease is Z15.89. The full clinical description is "Genetic susceptibility to other disease". Z15.89 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Z15.89 mean?

ICD-10-CM code Z15.89 represents “Genetic susceptibility to other 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 Z15.89 a billable code?

Yes, Z15.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Z15.89 in?

Z15.89 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).

What codes cannot be used with Z15.89?

Z15.89 has Excludes1 notes indicating codes that cannot be used together with it, including: chromosomal anomalies (Q90-Q99).

Are additional codes required with Z15.89?

Yes, when using Z15.89, also report: code, if applicable, for any associated family history of the disease (Z80-Z84).

What SNOMED CT codes does Z15.89 map to?

Z15.89 maps to 26 SNOMED CT concepts: 725150008, 725151007, 1172892009, 1197415001, 725432008, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Z15.89?

Z15.89 is linked to 1 UMLS Concept Unique Identifier: C1455996. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Z15.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like genetic susceptibility to other 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 Z15.89?

There is no direct ICD-11 mapping available for Z15.89 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.