Q69.9
BillablePolydactyly, 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 mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(281)
SNOMED CT
- Macroencephaly9740002
- Megalencephaly9740002
- Dandy-Walker deformity14447001
- Dandy-Walker malformation14447001
- Dandy-Walker syndrome14447001
- Congenital dilatation of colon24291004
- Congenital megacolon24291004
- Potter facies24814002
- Potter's facies24814002
- Arachnoid cyst33595009
- Cortical blindness68574006
- Majewski-type short rib polydactyly syndrome72922008
- Short rib-polydactyly syndrome, Majewski type72922008
- Short-rib syndrome, type II72922008
- Type II short rib polydactyly syndrome72922008
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Congenital abnormal shape of rib92943002
- Congenital misshapen rib92943002
- Mis-shapen ribs92943002
- Congenital hypoplasia of tibia93298007
- Congenital short tibia93298007
- Sensorineural hearing loss of bilateral ears194424005
- Sensorineural hearing loss of both ears194424005
- Hexadactyly201698009
- Congenital absence of the kidney204942005
- Renal agenesis204942005
- Cleft foot205358006
- Lobster claw foot205358006
- Split foot205358006
- Short rib polydactyly syndrome205484001
- Multinodular goiter237570007
- Multinodular goitre237570007
- Multiple thyroid nodules237570007
- Thyroid goiter multinodular237570007
- Thyroid goitre multinodular237570007
- Congenital anomaly of the meninges253199003
- Congenital malformation of the meninges253199003
- Short rib dysplasia254050009
- Short rib syndrome254050009
- Naumoff-type short rib polydactyly syndrome254051008
- Type III short rib polydactyly syndrome254051008
- Verma-Naumoff short rib polydactyly syndrome254051008
- Beemer-Langer type short rib polydactyly syndrome254052001
- Type IV short rib polydactyly syndrome254052001
- Mullerian remnant264491001
- Deformity of sternum298727009
- Hereditary disorder of lymphatic system363190001
- Accessory digit367506006
- Polydactyly367506006
- Supernumerary digit367506006
- Congenital funnel chest391982004
- Congenital pectus excavatum391982004
- Cobbler's chest391987005
- Funnel chest391987005
- Pectus excavatum391987005
- Pectus recurvatum391987005
- Trichterbrust391987005
- Pectus deformity of chest444693004
- Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation702407009
- McKusick Kaufman syndrome702407009
- Mirror polydactyly, vertebral segmentation and limb defect syndrome715523005
- Holoprosencephaly and postaxial polydactyly syndrome716091000
- Pseudotrisomy 13 syndrome716091000
- Bilateral hypoplasia of tibia and postaxial polydactyly syndrome716741008
- Hypoplastic tibia and postaxial polydactyly syndrome716741008
- Werner mesomelic syndrome716741008
- Brain malformation, congenital heart disease, postaxial polydactyly syndrome717943008
- Goossens Devriendt syndrome717943008
- Oliver syndrome721017000
- Postaxial polydactyly and intellectual disability syndrome721017000
- Hirschsprung disease with deafness and polydactyly syndrome721221000
- Santos Mateus Leal syndrome721221000
- Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome721970009
- MPPH (megalencephaly, polymicrogyria, polydactyly, hydrocephalus) syndrome722036008
- MPPH syndrome722036008
- Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome722036008
- Daneman Davy Mancer syndrome723409007
- Multinodular goiter, cystic kidney, polydactyly syndrome723409007
- Multinodular goitre, cystic kidney, polydactyly syndrome723409007
- Thyroid, renal, digital anomaly syndrome723409007
- Saldino Noonan syndrome726032008
- Short rib polydactyly syndrome Saldino Noonan type726032008
- Short rib polydactyly syndrome type 1726032008
- Short rib polydactyly syndrome type I726032008
- Scalp defect postaxial polydactyly syndrome726629006
- Cortical blindness, intellectual disability, polydactyly syndrome732251003
- Absent tibia, polydactyly, arachnoid cyst syndrome733068001
- Holmes Collins syndrome733068001
- Czeizel Brooser syndrome733087007
- Polydactyly myopia syndrome733087007
- Pfeiffer Mayer syndrome733088002
- Preaxial polydactyly, colobomata, intellectual disability syndrome733088002
- Dandy-Walker malformation with postaxial polydactyly syndrome733094005
- Pierquin syndrome733094005
- Hyperphalangy763535005
- Supernumerary phalanx763535005
- Intellectual disability, polydactyly, uncombable hair syndrome763742008
- Kozlowski Krajewska syndrome763742008
- Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome763866005
- ADPKD - autosomal dominant polycystic kidney disease765330003
- Autosomal dominant polycystic kidney disease765330003
- Ectrodactyly polydactyly syndrome771177009
- Postaxial polydactyly, dental, vertebral anomalies syndrome773279006
- Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome782758009
- Cleft palate, Potter sequence, congenital heart anomalies, mesoaxial polydactyly, multiple malformations syndrome783159001
- Holzgreve Wagner Rehder syndrome783159001
- Holzgreve syndrome783159001
- Syndactyly, polydactyly, ear lobe syndrome783700001
- Congenital lymphangiectases788292004
- Congenital lymphangiectasia788292004
- Congenital lymphangiectasis788292004
- Congenital anomaly of lobe of ear840482005
- Developmental defect of ear lobe840482005
- SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome1172635005
- Split-foot malformation, mesoaxial polydactyly syndrome1172635005
- Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome1172635005
- Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome1187115008
- Mirror-image polydactyly1255267007
- Short rib polydactyly syndrome type 51279843003
- Short rib polydactyly syndrome type V1279843003
UMLS
- Accessory digitC0152427
- HyperdactyliesC0152427
- HyperdactylyC0152427
- More than five fingers or toes on hands or feetC0152427
- Multiple digitsC0152427
- POLYDACTYLYC0152427
- PolydactyliaC0152427
- PolydactyliasC0152427
- PolydactyliesC0152427
- PolydactylismC0152427
- PolydactylismsC0152427
- PolydactylyC0152427
- Polydactyly (disorder)C0152427
- Polydactyly, unspecifiedC0152427
- Polydactyly, unspecified digitsC0152427
- Supernumerary digitC0152427
- Supernumerary digit(s) NOSC0152427
- Supernumerary digitsC0152427
- polydactyliaC0152427
- polydactylismC0152427
- polydactylyC0152427
- supernumerary digitC0152427
- supernumerary digitsC0152427
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.