2027 ICD-10-CM Diagnosis Code Z15.89Genetic susceptibility to other disease

ICD-10-CM Codes›Z00–Z99›Z14-Z15›Z15

ICD-10-CM Z15.89
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

Z15.89 is a billable ICD-10-CM diagnosis code for genetic susceptibility to other disease. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 951. The code is not accepted as a principal diagnosis by the Medicare Code Editor and exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Genetic susceptibility to disease.

Code Identity

ICD-10-CM Code
Z15.89
Billable Status
Yes — Valid for Submission
Code Describes
Genetic susceptibility to other disease
Short Description
Genetic susceptibility to other disease
Same as the full description in the CMS dataset.
Parent Code
Z15.8
Genetic susceptibility to other disease

Code Classification

ChapterZ00–Z99Factors influencing health status and contact with health services
SectionZ14-Z15Genetic carrier and genetic susceptibility to disease
CategoryZ15Genetic susceptibility to disease
This CodeZ15.89Genetic susceptibility to other disease

Code EditsBilling

Medicare Code Editor checks that affect claim validity for Z15.89.

Unacceptable principal diagnosis
There are selected codes that describe a circumstance which influences an individual's health status but not a current illness or injury, or codes that are not specific manifestations but may be due to an underlying cause. These codes are considered unacceptable as a principal diagnosis.

Present on Admission (POA)Billing

Z15.89 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Genetic carrier and genetic susceptibility to disease (Z14-Z15).

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to IL23R deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency
  • Genetic susceptibility to cardiovascular disorder
  • Genetic susceptibility to genetic disorder
  • Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation
  • Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation
  • Malignant hyperthermia genetic susceptibility
  • Mendelian susceptibility to mycobacterial disease
  • Mendelian susceptibility to mycobacterial disease due to complete IL12RB1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency
  • Predisposition to invasive fungal disease due to CARD9 deficiency
  • Predisposition to severe viral infection due to IRF7 deficiency
  • Susceptibility to infection due to TYK2 deficiency
  • Uncertain genetic susceptibility to malignant hyperthermia due to CACNA1S gene mutation
  • Uncertain malignant hyperthermia predisposition due to RyR1 gene mutation
  • X-linked mendelian susceptibility to mycobacterial disease

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to Z15.89: its own notes plus those printed at Z15 and Chapter 21. A note printed at a category, block or chapter applies to every code under it.

Includes

Further defines, or gives examples of, the content of the category.

From Z15 Genetic susceptibility to disease applies to 14 codes
  • confirmed abnormal gene

Excludes1

Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.

From Z15 Genetic susceptibility to disease applies to 14 codes
  • chromosomal anomalies (Q90-Q99)

Use Additional Code

Add a second code, after this one, to fully describe the condition.

From Z15 Genetic susceptibility to disease applies to 14 codes
  • code, if applicable, for any associated family history of the disease (Z80-Z84)

Notes

General instructions on how these codes are used.

From Chapter 21 (Z00-Z99) Factors influencing health status and contact with health services applies to 1,425 codes
  • Z codes represent reasons for encounters. A corresponding procedure code must accompany a Z code if a procedure is performed. Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00-Y89 are recorded as 'diagnoses' or 'problems'. This can arise in two main ways:
  • (a) When a person who may or may not be sick encounters the health services for some specific purpose, such as to receive limited care or service for a current condition, to donate an organ or tissue, to receive prophylactic vaccination (immunization), or to discuss a problem which is in itself not a disease or injury.
  • (b) When some circumstance or problem is present which influences the person's health status but is not in itself a current illness or injury.

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Referenced in Other NotesGuidance

Instructional notes printed at other codes that name Z15.89, its category, or a range that includes it.

Use Additional Code 1

These codes say to use an additional code from the note, and Z15.89 is one of the codes named.

  • Z40.0 Encounter for prophylactic surgery for risk factors related to malignant neoplasms
    code to identify risk factor, such as genetic susceptibility to malignant neoplasm Z15.- names Z15.-, which includes this code

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR FAC029
Genetic susceptibility to disease
Default principal diagnosis: inpatient No · outpatient No

Convert Z15.89 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
V84.89 Genetic suscept dis NEC
Exact Match The mapping is direct, with no qualifiers.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2026No changes
FY 2027CurrentCurrent code set, no changesEffective October 1, 2026 through September 30, 2027.

Questions About Z15.89Overview

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 (sometimes written as Z1589). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is Z15.89 (Genetic susceptibility to other disease) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report genetic susceptibility to other disease on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

What MS-DRG does Z15.89 group to?

On inpatient claims, genetic susceptibility to other disease maps to MS-DRG 951 (other Factors Influencing Health Status), which carries a relative weight of 0.5574. Higher weights mean higher Medicare reimbursement.

Can Z15.89 be a principal diagnosis?

No. The Medicare Code Editor rejects this code as a principal diagnosis because genetic susceptibility to other disease describes a circumstance that influences health status rather than a current illness. Report it as a secondary diagnosis.

Is Z15.89 exempt from POA reporting?

Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for genetic susceptibility to other disease on inpatient claims. The code appears in the Genetic carrier and genetic susceptibility to disease (Z14-Z15) range of the CMS exempt list.