Q69.9
BillablePolydactyly, unspecified
Polydactyly, unspecified
Status
Billable / Specific
Parent Code
Q69Coding 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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
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
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.
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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.