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ICD-10-CM 2027 diagnosis code

Q86.2Dysmorphism due to warfarin

✓ Billable / specificPOA exempt

Q86.2 is a valid, billable ICD-10-CM code for dysmorphism due to warfarin. It can be reported on claims for dates of service from October 1, 2026 – September 30, 2027.

Code unchanged since ICD-10-CM took effect on October 1, 2015. Source: official FY2027 ICD-10-CM release from CDC/NCHS and CMS. Page updated September 29, 2026. About our data

About Q86.2

Q86.2 is the ICD-10-CM diagnosis code for Dysmorphism due to warfarin. It belongs to category Q86 (congenital malformation syndromes due to known exogenous causes, not elsewhere classified), block Q80-Q89 (other congenital malformations) and chapter 17 (congenital malformations, deformations, chromosomal abnormalities, and genetic disorders). It is billable, so it can be reported on its own for dates of service from October 1, 2026 through September 30, 2027.

Within Q86 (congenital malformation syndromes due to known exogenous causes, not elsewhere classified), Q86.2 is specifically for Dysmorphism due to warfarin. Related codes cover fetal alcohol syndrome (dysmorphic) (Q86.0), fetal hydantoin syndrome (Q86.1) and other congenital malformation syndromes due to known exogenous causes (Q86.8).

It is not a CC or MCC, so as a secondary diagnosis it doesn't change the MS-DRG severity level.

In MS-DRG v44.0, it is part of the grouping logic for DRG 794 (Neonate with Other Significant Problems, relative weight 1.4935), in MDC 15 (Newborns and Other Neonates with Conditions Originating in the Perinatal Period), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.

It is exempt from present-on-admission (POA) reporting, so no POA indicator is required.

It has been part of ICD-10-CM since the code set took effect on October 1, 2015 and hasn't changed since.

Before ICD-10, this condition was coded in ICD-9-CM as 760.79 (other noxious influences affecting fetus or newborn via placenta or breast milk).

Notes that apply from higher levels

Instructions written at a parent level also apply to Q86.2.

› From Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
Excludes2
  • iodine-deficiency-related hypothyroidism (E00-E02)
  • nonteratogenic effects of substances transmitted via placenta or breast milk (P04.-)

Broader instructions also apply from Chapter 17: Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders.

Alphabetic index entries

2 entries

Terms in the official ICD-10-CM index that lead to Q86.2.

Codes whose notes reference Q86.2

MS-DRG v44.0 grouping

All DRGs →

Inpatient MS-DRGs this diagnosis can group to, as the principal or a secondary diagnosis, depending on the rest of the claim.

MDC 15 · Newborns and Other Neonates with Conditions Originating in the Perinatal Period

ICD-9-CM equivalent

Converter →
  • 760.79Other noxious influences affecting fetus or newborn via placenta or breast milkapproximate

From the CMS 2018 General Equivalence Mappings (GEMs), the final GEMs release.

Code history

  1. 2016
  2. 2017
  3. 2018
  4. 2019
  5. 2020
  6. 2021
  7. 2022
  8. 2023
  9. 2024
  10. 2025
  11. 2026
  12. 2027
  • FY2016 (effective 10/1/2015): Added (first year of ICD-10-CM)
  • No changes since FY2016.

Common questions about Q86.2

Is Q86.2 billable?

Yes. Q86.2 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).

Can Q86.2 be used as a principal diagnosis?

Yes. The Medicare Code Editor doesn't restrict Q86.2 as a principal diagnosis.

Is Q86.2 a CC or MCC?

No. Q86.2 is neither a CC nor an MCC under MS-DRG v44.0.

What DRG does Q86.2 group to?

Q86.2 is used in the MS-DRG v44.0 logic for MS-DRG 794 (Neonate with Other Significant Problems). Which one applies depends on whether it is the principal diagnosis and on the rest of the claim.

What is the ICD-9 code for Q86.2?

The CMS General Equivalence Mappings map Q86.2 to ICD-9-CM 760.79.