Q70.9
BillableSyndactyly, unspecified
Syndactyly, unspecified
Status
Billable / Specific
Parent Code
Q70Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Symphalangy 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
- 2q partial trisomy syndrome5982001
- Congenital cleft hand13624003
- Lobster claw hand13624003
- Lobster-claw hand13624003
- Clinodactyly17268007
- Congenital clinodactyly17268007
- Pendular nystagmus35743001
- Congenital nystagmus64635004
- Acrocephalosyndactyly type 570410008
- Acrocephalosyndactyly type V70410008
- Pfeiffer syndrome70410008
- Pfeiffer-type acrocephalosyndactyly70410008
- Ankylosis of proximal interphalangeal joint202314000
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- Cleft hand with syndactyly205266000
- Proximal interphalangeal joint symphalangism205280007
- Distal interphalangeal joint symphalangism205281006
- Brachymesophalangia205317004
- Ectodermal dysplasia, syndactyly and pili torti239024004
- Telecanthus246803005
- Congenital anomaly of the eyebrow253206006
- Congenital malformation of the eyebrow253206006
- Syndactyly of thumb253972001
- Symphalangism253975004
- Acrocephalosyndactyly268262006
- Congenital webbing of digits373413006
- Syndactylia373413006
- Syndactylism373413006
- Syndactylus373413006
- Syndactyly373413006
- Congenital bony fusion of phalanges373427001
- Syndactyly type 1715723008
- Syndactyly type 2715724002
- Synpolydactyly715724002
- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome717914000
- Frydman Cohen Karmon syndrome717914000
- Haas type syndactyly719158007
- Syndactyly type 4719158007
- Syndactyly type 5719159004
- Aphalangy and syndactyly with microcephaly syndrome720498007
- Cenani Lenz syndactyly720633009
- Cenani Lenz syndrome720633009
- Cenani syndactyly720633009
- Syndactyly type 7720633009
- STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome723581006
- STAR syndrome723581006
- Syndactyly, telecanthus, anogenital and renal malformation syndrome723581006
- Bonneau syndrome724066002
- Polysyndactyly and cardiac malformation syndrome724066002
- Mesoaxial synostotic syndactyly with phalangeal reduction syndrome724170007
- Syndactyly Malik Percin type724170007
- Syndactyly type 9724170007
- Duplication of chromosome 2726340005
- Partial trisomy of chromosome 2726340005
- Learman syndrome732955001
- Symphalangism with multiple anomalies of hands and feet732955001
- Symphalangism with multiple anomalies of hands and feet syndrome732955001
- Brachydactyly and distal symphalangism syndrome732956000
- Sillence syndrome732956000
- Duplication of eyebrow and syndactyly syndrome733070005
- Eyebrow duplication syndactyly syndrome733070005
- Ectodermal dysplasia syndactyly syndrome771335004
- FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome774070008
- Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome774070008
- FATCO syndrome783156008
- Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome783156008
- Hecht Scott syndrome783156008
- Synactyly, camptodactyly and clinodactyly of fifth fingers, bifid halluces syndrome783553008
- Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome783553008
- Wahab syndrome783553008
- Syndactyly, nystagmus syndrome due to 2q31.1 microduplication783562005
- Syndactyly, nystagmus syndrome due to trisomy 2q31.1783562005
- Syndactyly, polydactyly, ear lobe syndrome783700001
- Congenital anomaly of lobe of ear840482005
- Developmental defect of ear lobe840482005
- Bilateral distal interphalangeal joint symphalangism890351008
- Distal symphalangism of bilateral distal interphalangeal joints890351008
- Distal symphalangism of both distal interphalangeal joints890351008
- Bilateral proximal symphalangism890425005
- Proximal symphalangism of bilateral fingers890425005
- Proximal symphalangism of fingers of both hands890425005
- Congenital clinodactyly of finger1003620005
- Congenital crooked finger1003620005
- Congenital clinodactyly of fifth digit of hand1003621009
- Congenital clinodactyly of little finger1003621009
- Pfeiffer syndrome type 11003877009
- Pfeiffer syndrome type 21003916008
- Pfeiffer syndrome type 31003918009
- Bilateral webbed fingers1010618000
- Syndactyly of fingers of bilateral hands1010618000
- Syndactyly of fingers of both hands1010618000
- Congenital hypoplasia of nail unit1144442009
- Proximal interphalangeal joint symphalangism Cushing type1162837001
- Symphalangism Cushing type1162837001
- Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome1279835008
- Ankylosis of joint of finger of left hand15726601000119105
- Ankylosis of joint of finger of right hand15726561000119105
- Bilateral syndactyly of toes308561000119101
- Syndactyly of toes of bilateral feet308561000119101
- Syndactyly of toes of both feet308561000119101
- Syndactyly of fingers of left hand308541000119100
- Syndactyly of fingers of right hand308551000119103
- Syndactyly of toes of left foot308571000119107
- Syndactyly of toes of right foot308581000119105
UMLS
- Congenital webbing of digitsC0039075
- SyndactyliaC0039075
- SyndactyliasC0039075
- SyndactyliesC0039075
- SyndactylismC0039075
- SyndactylusC0039075
- SyndactylyC0039075
- Syndactyly (disorder)C0039075
- Syndactyly, unspecifiedC0039075
- Webbed fingers or toesC0039075
- symphalangismC0039075
- syndactyliaC0039075
- syndactyliesC0039075
- syndactylismC0039075
- syndactylyC0039075
- SymphalangismC5848178
- Symphalangism (disorder)C5848178
- Symphalangy NOSC5848178
Frequently Asked Questions
What is the ICD-10 code for syndactyly, unspecified?
The ICD-10-CM code for syndactyly, unspecified is Q70.9. The full clinical description is "Syndactyly, unspecified". Q70.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q70.9 mean?
ICD-10-CM code Q70.9 represents "Syndactyly, 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 Q70.9 a billable code?
Yes, Q70.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q70.9 in?
Q70.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q70.9 map to?
Q70.9 maps to 59 SNOMED CT concepts: 5982001, 268262006, 70410008, 204712000, 15726601000119105, and 54 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q70.9?
Q70.9 is linked to 2 UMLS Concept Unique Identifiers: C0039075, C5848178. 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.