Z15.89
BillableGenetic susceptibility to other disease
Genetic susceptibility to other disease
Coding Notes
Includes
Conditions included under this code
- confirmed abnormal gene
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- chromosomal anomalies (Q90-Q99)
Use Additional Code
Additional codes that should follow this code
- code, if applicable, for any associated family history of the disease (Z80-Z84)
Also Known As / Clinical Terms
SNOMED CT
- Dense body defect234474009
- Storage pool deficiency234474009
- Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency716869006
- Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency716869006
- Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR1 deficiency718230004
- Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency718230004
- X-linked mendelian susceptibility to mycobacterial disease719814009
- Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR2 deficiency721876004
- Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency721876004
- Mendelian susceptibility to mycobacterial disease due to complete IL12B deficiency721877008
- Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency721877008
- Mendelian susceptibility to mycobacterial disease due to complete ISG15 (interferon stimulated gene 15) deficiency723384004
- Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency723384004
- Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency723384004
- Mendelian susceptibility to mycobacterial disease due to partial IRF8 (interferon regulatory factor 8) deficiency723385003
- Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency723385003
- Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency723385003
- Mendelian susceptibility to mycobacterial disease due to partial STAT1 (signal transducer and activator of transcription 1) deficiency723386002
- Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency723386002
- Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency723386002
- Familial platelet disorder with associated myeloid malignancy725034002
- Familial platelet syndrome with predisposition to acute myelogenous leukaemia725034002
- Familial platelet syndrome with predisposition to acute myelogenous leukemia725034002
- Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency725150008
- Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency725150008
- Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency725151007
- Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency725151007
- Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency725432008
- Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency725432008
- Genetic susceptibility to malignant hyperthermia890189007
- Malignant hyperthermia genetic susceptibility890189007
- Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation1004155003
- Uncertain genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation1004155003
- Genetic susceptibility to malignant hyperthermia due to RYR1 (ryanodine receptor 1) gene mutation positive1010400009
- Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation1010400009
- Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation positive1010400009
- Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation1141749000
- Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation positive1141749000
- Malignant hyperthermia predisposition due to CACNA1S (calcium voltage-gated channel subunit alpha1 S) gene mutation positive1141749000
- Uncertain genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation1142134000
- Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation1142134000
- Autosomal recessive MSMD (mendelian susceptibility to mycobacterial disease) due to complete RORgamma receptor mutation1172892009
- Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation1172892009
- Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation1172892009
- Autosomal recessive primary immunodeficiency due to RORC mutation1172892009
- MSMD - mendelian susceptibility to mycobacterial disease1172895006
- Mendelian susceptibility to mycobacterial disease1172895006
- Mendelian susceptibility to mycobacterial infection1172895006
- Invasive candidiasis, deep dermatophytosis syndrome1186719000
- Predisposition to invasive fungal disease due to CARD9 deficiency1186719000
- Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency1186719000
- Autosomal recessive hyper-IgE (immunoglobulin E) syndrome due to TYK2 deficiency1197415001
- Susceptibility to infection due to TYK2 deficiency1197415001
- Susceptibility to infection due to tyrosine kinase 2 deficiency1197415001
- Predisposition to severe viral infection due to IRF7 deficiency1269234000
- Predisposition to severe viral infection due to interferon regulatory factor 7 deficiency1269234000
- Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency1279842008
- Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial janus kinase 1 deficiency1279842008
- Genetic susceptibility to cardiovascular disorder752301151000119107
- Genetic susceptibility to genetic disorder71951000119107
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 you should also code: 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.
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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.