2027 ICD-10-CM Diagnosis Code Q91.3Trisomy 18, unspecified
ICD-10-CM Codes›Q00-Q99›Q90-Q99›Q91
- Billable — Valid for Submission
- CC — Complication or Comorbidity
- POA Exempt
- Chronic Condition
Q91.3 is a billable ICD-10-CM diagnosis code for trisomy 18, unspecified. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 884. As a secondary diagnosis, it counts as a complication or comorbidity (CC) and moves an inpatient stay to a higher severity level within its MS-DRG family. It does not count, however, when the principal diagnosis is one of 68 closely related codes. The code is exempt from POA reporting. Coders also document this condition as 18q partial trisomy syndrome. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Chromosomal abnormalities.
Q91.3 does not risk-adjust for Medicare Advantage under the CMS-HCC V28 model. It still risk-adjusts in the RxHCC Part D (V08) category 148 for payment year 2027.
Code Identity
Code Classification
Present on Admission (POA)Billing
Q91.3 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Chromosomal abnormalities, not elsewhere classified (Q90-Q99).
Medicare Risk Adjustment (HCC)Billing
Q91.3 does not risk-adjust for Medicare Advantage under the CMS-HCC V28 model, but it maps to payment categories in the other CMS models shown below.
Source: CMS Payment Year 2027 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- 18q partial trisomy syndrome
- Complete trisomy 18 syndrome
- Distal trisomy 18q
- Partial trisomy of chromosome 18
- Proximal duplication of long arm of chromosome 18
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to Q91.3: its own notes plus those printed at block Q90-Q99 and Chapter 17. A note printed at a category, block or chapter applies to every code under it.
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- mitochondrial metabolic disorders (E88.4-)
Notes
General instructions on how these codes are used.
- Codes from this chapter are not for use on maternal records
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name Q91.3, its category, or a range that includes it.
Excludes1 4
These codes carry an Excludes1 note naming Q91.3: they are not reported together with it, unless the two conditions are unrelated.
- E25 Adrenogenital disorders
- Block Q50-Q56 Congenital malformations of genital organs
- Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
- Z15 Genetic susceptibility to disease
Code First 1
These codes say to code first a condition named in the note, and Q91.3 is one of the conditions named.
- D84.81 Immunodeficiency due to conditions classified elsewhere
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.
Clinical InformationClinical
Complete Trisomy 18 Syndrome
a constellation of symptoms that occur as a result of the presence of a complete third copy of the 18th chromosome. characteristics include profound mental retardation and severe malformations. individuals with this syndrome rarely live past one year.
Patient EducationClinical
Genetic Disorders
Genetic disorders are health conditions caused by changes (also called mutations or variants) in your genes. Genes are parts of DNA found in your cells that carry instructions for how your body grows, develops, and functions. Many genes tell your body how to make proteins, which are needed for your body to work properly.
The full article covers:
- What are genetic disorders?
- What causes genetic disorders?
- What are the types of genetic disorders?
- What are the different ways a genetic disorder can be inherited?
- How are genetic disorders diagnosed?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q91.3 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q91.3Overview
What is the ICD-10 code for trisomy 18, unspecified?
The ICD-10-CM code for trisomy 18, unspecified is Q91.3 (sometimes written as Q913). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is Q91.3 (Trisomy 18 and Trisomy 13) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report trisomy 18, unspecified on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does Q91.3 group to?
When trisomy 18, unspecified is the principal diagnosis on an inpatient stay, it groups to MS-DRG 884 (organic Disturbances and Intellectual Disability), which carries a relative weight of 1.5998. Higher weights mean higher Medicare reimbursement.
Is Q91.3 a CC or MCC?
CMS lists Q91.3 as a CC (complication or comorbidity) for FY 2027. Reported as a secondary diagnosis, it moves the inpatient stay to a higher-weighted DRG within its severity family. It does not count when the principal diagnosis is one of the 68 closely related codes in its exclusion list.
Is Q91.3 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 trisomy 18, unspecified on inpatient claims. The code appears in the Chromosomal abnormalities, not elsewhere classified (Q90-Q99) range of the CMS exempt list.
Does Q91.3 risk-adjust for Medicare Advantage payment?
Not for Medicare Advantage: Q91.3 maps to no category in the CMS-HCC V28 model. It still risk-adjusts in the RxHCC Part D (V08) category 148 (Mild or Unspecified Intellectual Disability/Developmental Disorder).