2027 ICD-10-CM Diagnosis Code Q69.9Polydactyly, unspecified
ICD-10-CM Codes›Q00-Q99›Q65-Q79›Q69
- Billable — Valid for Submission
- POA Exempt
- Chronic Condition
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
Code Classification
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.
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 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.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Hexadactylism Q69.9
Multiple, multiplex See Also: condition;
digits (congenital) Q69.9
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
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.
Code HistoryHistory
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.