2027 ICD-10-CM Diagnosis Code Q69.9Polydactyly, unspecified

ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q69

ICD-10-CM Q69.9
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

Q69.9 is a billable ICD-10-CM diagnosis code for polydactyly, unspecified. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 564 through 566. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Musculoskeletal congenital conditions.

Code Identity

ICD-10-CM Code
Q69.9
Billable Status
Yes — Valid for Submission
Code Describes
Polydactyly, unspecified
Short Description
Polydactyly, unspecified
Same as the full description in the CMS dataset.
Parent Code
Polydactyly

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ65-Q79Congenital malformations and deformations of the musculoskeletal system
CategoryQ69Polydactyly
This CodeQ69.9Polydactyly, unspecified

Present on Admission (POA)Billing

Q69.9 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Congenital malformations and deformations of the musculoskeletal system (Q65-Q79).

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Absent tibia, polydactyly, arachnoid cyst syndrome
  • Arachnoid cyst
  • Autosomal dominant polycystic kidney disease
  • Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
  • Brain malformation, congenital heart disease, postaxial polydactyly syndrome
  • Congenital abnormal shape of rib
  • Congenital anomaly of lobe of ear
  • Congenital dilatation of colon
  • Congenital goiter
  • Congenital hypoplasia of tibia
  • Congenital lymphangiectasia
  • Congenital pectus excavatum
  • Cortical blindness
  • Cortical blindness, intellectual disability, polydactyly syndrome
  • Dandy-Walker malformation with postaxial polydactyly syndrome
  • Dandy-Walker syndrome
  • Ectrodactyly polydactyly syndrome
  • Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome
  • Hereditary disorder of lymphatic system
  • Hexadactyly
  • Hirschsprung disease with deafness and polydactyly syndrome
  • Holoprosencephaly and postaxial polydactyly syndrome
  • Holzgreve syndrome
  • Hyperphalangy
  • Hypoplastic tibia and postaxial polydactyly syndrome
  • Intellectual disability, polydactyly, uncombable hair syndrome
  • Macroencephaly
  • McKusick Kaufman syndrome
  • Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome
  • Micromelia
  • Mirror polydactyly, vertebral segmentation and limb defect syndrome
  • Mirror-image polydactyly
  • Mullerian remnant
  • Multinodular goiter
  • Multinodular goiter, cystic kidney, polydactyly syndrome
  • Oliver syndrome
  • Pectus deformity of chest
  • Pectus excavatum
  • Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome
  • Polydactyly
  • Polydactyly myopia syndrome
  • Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome
  • Postaxial polydactyly, dental, vertebral anomalies syndrome
  • Potter's facies
  • Preaxial polydactyly, colobomata, intellectual disability syndrome
  • Renal agenesis
  • Scalp defect postaxial polydactyly syndrome
  • Short rib dysplasia
  • Short rib polydactyly syndrome
  • Short rib polydactyly syndrome Saldino Noonan type
  • Short rib polydactyly syndrome type 5
  • Short rib-polydactyly syndrome, Majewski type
  • Split foot
  • Split-foot malformation, mesoaxial polydactyly syndrome
  • Syndactyly, polydactyly, ear lobe syndrome
  • Thyroid follicular nodular disease
  • Type III short rib polydactyly syndrome
  • Type IV short rib polydactyly syndrome

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to Q69.9: its own notes plus those printed at Chapter 17. A note printed at a category, block or chapter applies to every code under it.

Applicable To

Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.

  • Supernumerary digit(s) NOS

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.

From Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
  • inborn errors of metabolism (E70-E88)

Notes

General instructions on how these codes are used.

From Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
  • 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 Q69.9, its category, or a range that includes it.

Excludes1 2

These codes carry an Excludes1 note naming Q69.9: they are not reported together with it, unless the two conditions are unrelated.

  • Q74 Other congenital malformations of limb(s)
    polydactyly (Q69.-) names Q69.-, which includes this code
  • M20 Acquired deformities of fingers and toes
    congenital deformities and malformations of fingers and toes (Q66.-, Q68-Q70, Q74.-) names Q68-Q70, 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 MAL008
Musculoskeletal congenital conditions
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Polydactyly

    a congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.

Patient EducationClinical

Birth Defects

A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.

The full article covers:

  • What are birth defects?
  • What causes birth defects?
  • Who is at risk of having a baby with birth defects?
  • How are birth defects diagnosed?
  • What are the treatments for birth defects?
  • Can birth defects be prevented?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert Q69.9 to ICD-9-CMHistory

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

ICD-9-CM
755.00 Polydactyly NOS
Approximate The match is approximate rather than exact.

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 Q69.9Overview

What is the ICD-10 code for polydactyly, unspecified?

The ICD-10-CM code for polydactyly, unspecified is Q69.9 (sometimes written as Q699). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is Q69.9 (Polydactyly) a billable code?

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

What MS-DRG does Q69.9 group to?

When polydactyly, unspecified is the principal diagnosis on an inpatient stay, it groups to MS-DRG 564, 566, 565, with relative weights from 0.7374 to 1.4909 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q69.9 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 polydactyly, unspecified on inpatient claims. The code appears in the Congenital malformations and deformations of the musculoskeletal system (Q65-Q79) range of the CMS exempt list.

What is the ICD-9 equivalent of Q69.9?

Under the General Equivalence Mappings, polydactyly, unspecified converts to ICD-9-CM 755.00 (polydactyly NOS). The mapping is approximate, so confirm the match fits the documentation.