AutoICD API

Q69.9

Billable

Polydactyly, unspecified

Polydactyly, unspecified

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Supernumerary digit(s) NOS

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(281)

SNOMED CT

Clinical Terms

  • Thyroid goiter multinodular
  • Deformity of sternum
  • Short rib polydactyly syndrome type 1
  • Short-rib syndrome, type II
  • Congenital absence of the kidney
  • Lobster claw foot
  • Micromelus
  • Postaxial polydactyly and intellectual disability syndrome
  • Split-foot malformation, mesoaxial polydactyly syndrome
  • Congenital dilatation of colon
  • supernumerary digit
  • Holzgreve Wagner Rehder syndrome
  • Potter's facies
  • Saldino Noonan syndrome
  • Type IV short rib polydactyly syndrome
  • Micromelic dwarf
  • Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
  • Hereditary disorder of lymphatic system
  • Congenital lymphangiectasia
  • Mullerian remnant
  • Congenital misshapen rib
  • Pectus deformity of chest
  • SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome
  • Short rib polydactyly syndrome type I
  • Hexadactyly
  • Potter facies
  • Congenital abnormal shape of rib
  • Congenital short tibia
  • Majewski-type short rib polydactyly syndrome
  • Multiple thyroid nodules
  • Polydactyly myopia syndrome
  • Supernumerary digits
  • Oliver syndrome
  • Hyperdactyly
  • Supernumerary digit(s) NOS
  • Congenital megacolon
  • Funnel chest
  • Beemer-Langer type short rib polydactyly syndrome
  • Polydactylies
  • Trichterbrust
  • Thyroid, renal, digital anomaly syndrome
  • Autosomal dominant polycystic kidney disease
  • Postaxial polydactyly, dental, vertebral anomalies syndrome
  • Congenital anomaly of the meninges
  • More than five fingers or toes on hands or feet
  • Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation
  • Mis-shapen ribs
  • Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome
  • Czeizel Brooser syndrome
  • ADPKD - autosomal dominant polycystic kidney disease
  • Intellectual disability, polydactyly, uncombable hair syndrome
  • Congenital hypoplasia of tibia
  • Short rib polydactyly syndrome
  • Cleft foot
  • Mirror-image polydactyly
  • MPPH (megalencephaly, polymicrogyria, polydactyly, hydrocephalus) syndrome
  • Congenital malformation of the meninges
  • Scalp defect postaxial polydactyly syndrome
  • McKusick Kaufman syndrome
  • Hyperphalangy
  • Congenital funnel chest
  • Multinodular goitre, cystic kidney, polydactyly syndrome
  • Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome
  • Short rib-polydactyly syndrome, Majewski type
  • Naumoff-type short rib polydactyly syndrome
  • Syndactyly, polydactyly, ear lobe syndrome
  • Holoprosencephaly and postaxial polydactyly syndrome
  • Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome
  • polydactylia
  • Werner mesomelic syndrome
  • Absent tibia, polydactyly, arachnoid cyst syndrome
  • Congenital lymphangiectasis
  • Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome
  • Bilateral hypoplasia of tibia and postaxial polydactyly syndrome
  • Cortical blindness, intellectual disability, polydactyly syndrome
  • Short rib polydactyly syndrome type 5
  • Sensorineural hearing loss of bilateral ears
  • polydactylism
  • Dandy-Walker malformation
  • Mirror polydactyly, vertebral segmentation and limb defect syndrome
  • Short rib polydactyly syndrome type V
  • Sensorineural hearing loss of both ears
  • Polydactylisms
  • Goossens Devriendt syndrome
  • Type III short rib polydactyly syndrome
  • Holmes Collins syndrome
  • Short rib polydactyly syndrome Saldino Noonan type
  • Dandy-Walker deformity
  • Macroencephaly
  • Dandy-Walker malformation with postaxial polydactyly syndrome
  • Polydactyly (disorder)
  • MPPH syndrome
  • Congenital anomaly of lobe of ear
  • Split foot
  • Polydactyly, unspecified digits
  • Preaxial polydactyly, colobomata, intellectual disability syndrome
  • Congenital pectus excavatum
  • Pfeiffer Mayer syndrome
  • Cleft palate, Potter sequence, congenital heart anomalies, mesoaxial polydactyly, multiple malformations syndrome
  • Pectus excavatum
  • Pierquin syndrome
  • Pseudotrisomy 13 syndrome
  • Multinodular goiter, cystic kidney, polydactyly syndrome
  • Multinodular goitre
  • Accessory digit
  • Micromelia
  • Pectus recurvatum
  • Type II short rib polydactyly syndrome
  • Multiple digits
  • Renal agenesis
  • Santos Mateus Leal syndrome
  • Hypoplastic tibia and postaxial polydactyly syndrome
  • Short rib dysplasia
  • Polydactylias
  • Megalencephaly
  • Brain malformation, congenital heart disease, postaxial polydactyly syndrome
  • Short rib syndrome
  • Supernumerary phalanx
  • Dandy-Walker syndrome
  • Congenital lymphangiectases
  • Hyperdactylies
  • Cortical blindness
  • Arachnoid cyst
  • Developmental defect of ear lobe
  • Multinodular goiter
  • Cobbler's chest
  • Nanomelia
  • Hirschsprung disease with deafness and polydactyly syndrome
  • Daneman Davy Mancer syndrome
  • Holzgreve syndrome
  • Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome
  • Ectrodactyly polydactyly syndrome
  • Verma-Naumoff short rib polydactyly syndrome
  • Kozlowski Krajewska syndrome
  • Thyroid goitre multinodular
Frequently Asked Questions
What is the ICD-10 code for polydactyly, unspecified?

The ICD-10-CM code for polydactyly, unspecified is Q69.9. The full clinical description is "Polydactyly, unspecified". Q69.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q69.9 mean?

ICD-10-CM code Q69.9 represents “Polydactyly, unspecified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q69.9 a billable code?

Yes, Q69.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q69.9 in?

Q69.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q69.9 map to?

Q69.9 maps to 59 SNOMED CT concepts: 765330003, 733068001, 367506006, 33595009, 1187115008, and 54 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q69.9?

Q69.9 is linked to 1 UMLS Concept Unique Identifier: C0152427. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q69.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like polydactyly, unspecified affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q69.9?

Q69.9 maps to the ICD-11 code: LB78.Z (Polydactyly, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.