Wahab syndrome
syndactylia
Pfeiffer syndrome type 1
Ankylosis of joint of finger of right hand
Pfeiffer syndrome
Syndactyly of toes of right foot
Pfeiffer-type acrocephalosyndactyly
Symphalangism with multiple anomalies of hands and feet syndrome
Learman syndrome
Proximal interphalangeal joint symphalangism Cushing type
Brachymesophalangia
Syndactyly, telecanthus, anogenital and renal malformation syndrome
Syndactyly type 4
Atresia ani
Aphalangy and syndactyly with microcephaly syndrome
Bilateral distal interphalangeal joint symphalangism
Syndactyly type 9
Syndactyly, nystagmus syndrome due to 2q31.1 microduplication
Aproctia
Symphalangism (disorder)
Cleft hand with syndactyly
Proximal symphalangism of bilateral fingers
Congenital malformation of the eyebrow
Polysyndactyly and cardiac malformation syndrome
Ankylosis of proximal interphalangeal joint
Duplication of eyebrow and syndactyly syndrome
Eyebrow duplication syndactyly syndrome
Proximal symphalangism of fingers of both hands
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome
Congenital bony fusion of phalanges
Frydman Cohen Karmon syndrome
Cenani Lenz syndrome
Syndactylias
Syndactyly of toes of both feet
Syndactyly of fingers of both hands
Bilateral syndactyly of toes
STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome
Lobster claw hand
Congenital nystagmus
Clinodactyly
Haas type syndactyly
Congenital clinodactyly of fifth digit of hand
Congenital webbing of digits
Congenital clinodactyly of finger
Syndactyly type 5
Sillence syndrome
Symphalangism with multiple anomalies of hands and feet
Syndactylus
STAR syndrome
Acrocephalosyndactyly type 5
Synactyly, camptodactyly and clinodactyly of fifth fingers, bifid halluces syndrome
Symphalangism Cushing type
Pfeiffer syndrome type 2
symphalangism
Hecht Scott syndrome
Webbed fingers or toes
Pendular nystagmus
Congenital crooked finger
syndactylies
Congenital atresia of anus
Syndactyly type 7
Cenani syndactyly
Pfeiffer syndrome type 3
Cenani Lenz syndactyly
Congenital hypoplasia of nail unit
Duplication of chromosome 2
Ankylosis of joint of finger of left hand
Syndactyly, polydactyly, ear lobe syndrome
Telecanthus
Ectodermal dysplasia syndactyly syndrome
Acrocephalosyndactyly
Syndactyly of toes of left foot
Imperforate anus
FATCO syndrome
Proximal interphalangeal joint symphalangism
Bonneau syndrome
Brachydactyly and distal symphalangism syndrome
Symphalangy NOS
Syndactyly, nystagmus syndrome due to trisomy 2q31.1
Distal symphalangism of both distal interphalangeal joints
Congenital clinodactyly of little finger
Syndactyly Malik Percin type
Congenital cleft hand
Syndactyly of fingers of left hand
Syndactyly (disorder)
Bilateral proximal symphalangism
Syndactyly type 1
Congenital anomaly of lobe of ear
Partial trisomy of chromosome 2
Bilateral webbed fingers
Ectodermal dysplasia, syndactyly and pili torti
Distal symphalangism of bilateral distal interphalangeal joints
Congenital imperforate anus
Lobster-claw hand
Syndactyly type 2
Syndactyly of fingers of right hand
Distal interphalangeal joint symphalangism
Syndactyly of fingers of bilateral hands
FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
Synpolydactyly
Acrocephalosyndactyly type V
Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome
Syndactyly of toes of bilateral feet
2q partial trisomy syndrome
Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome
Congenital clinodactyly
Congenital anomaly of the eyebrow
Syndactyly of thumb
Anal atresia
syndactylism
Mesoaxial synostotic syndactyly with phalangeal reduction syndrome
Developmental defect of ear lobe
Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome

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.

How does Q70.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like syndactyly, 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 Q70.9?

Q70.9 maps to the ICD-11 code: LB79.Z (Syndactyly, 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.