Hypoplasia of thumb
Generalized spacing of maxillary teeth
Transverse deficiency of upper limb
Congenital hypoplasia of fourth metacarpal bone
Congenital short fibula
Congenital hypoplasia of phalanx of middle finger
Deformity of metacarpal
Congenital hypoplasia of second metacarpal bone
Congenital hypoplasia of phalanx of little finger
Reinhardt Pfeiffer syndrome
Schmitt Gillenwater Kelly syndrome
Brachydactyly, scoliosis, carpal fusion syndrome
Congenital absence of humerus
Congenital hypoplasia of middle phalanx of index finger
Hypoplasia of radius
Reinhardt Pfeiffer mesomelic dysplasia
Congenital hypoplasia of middle phalanx of finger
Intrauterine amputation of upper limb
Short fifth metacarpal insulin resistance syndrome
Congenital hypoplasia of bone of radius and/or ulna
Congenital hypoplasia of phalanx of hand
Congenital abnormal shape of carpal bone
Congenital hypoplasia of radius
Shortened fifth metacarpal
Hypoplastic thumb
Congenital short humerus
Prata Liberal Goncalves syndrome
Congenital hypoplasia of index finger
Transverse arrest of the arm
Hypoplastic thumb-Blauth 5
Congenital hypoplasia of middle phalanx of ring finger
Hypoplasia of distal phalanx of little finger
Congenital hypoplastic carpal bone
Hypoplasia of distal phalanx of ring finger
Congenital absence of part of upper arm
Undergrowth of the thumb
Mesomelic dysplasia of hypoplastic ulna and fibula type
Hypoplasia of distal phalanx of index finger
Congenital hypoplasia of middle phalanx of middle finger
Congenital short ulna
Congenital hypoplasia of middle phalanx of little finger
Transverse deficiency of arm, upper arm level - short
Hyperphalangy
Congenital anomalies of elbow and upper arm
Hypoplasia of distal phalanx of hand
Congenital hypoplasia of little finger
Mesomelic dwarfism Reinhardt-Pfeiffer type
Congenital hypoplasia of humerus
Congenital hypoplasia of proximal phalanx of hand
Acrodysplasia scoliosis
Congenital short radius
Hypoplastic thumb-Blauth 3
Congenital hypoplasia of phalanx of ring finger
Congenital small metacarpal bone
Congenital misshapen carpal bone
Congenital hypoplasia of fifth metacarpal bone
Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome
Aplasia of lateral condyle of humerus
Deformity of carpal bone
Congenital absence of upper arm only
Triphalangeal thumb
Hypoplastic thumb-Blauth 4
Hypoplasia of distal phalanx of middle finger
Congenital hypoplasia of metacarpal bone
Longitudinal deficiency of phalanges of hand
Congenital hypoplasia of fibula
Congenital hypoplasia of third metacarpal bone
Proximal phocomelia of upper limb
Hypoplastic thumb-Blauth 2
Congenital hypoplasia of ulna
Congenital hypoplasia of carpal bone
Transverse deficiency of arm
Transverse deficiency of arm, upper arm level - long
Congenital hypoplasia of phalanx of index finger
Abnormally short fifth metacarpal
Congenital amputation of upper limb
Agenesis of humerus
Aplasia of humerus
Aplasia of lateral humeral condyle
Congenital hypoplasia of first metacarpal bone
Congenital hypoplasia of phalanx of thumb
Hypoplastic thumb-Blauth 1
Congenital hypoplasia of ring finger
Supernumerary phalanx
Congenital hypoplasia of middle finger
Generalised spacing of maxillary teeth
Longitudinal deficiency of metacarpal bone
Congenital hypoplasia of bone of forearm
Longitudinal deficiency of carpal bone
Congenital small carpal bone
Congenital hypoplasia of bone of hand
Congenital hypoplasia of proximal phalanx of thumb

Frequently Asked Questions

What is the ICD-10 code for other reduction defects of unspecified upper limb?

The ICD-10-CM code for other reduction defects of unspecified upper limb is Q71.899. The full clinical description is "Other reduction defects of unspecified upper limb". Q71.899 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q71.899 mean?

ICD-10-CM code Q71.899 represents “Other reduction defects of unspecified upper limb”. 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 Q71.899 a billable code?

Yes, Q71.899 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q71.899 in?

Q71.899 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q71.899 map to?

Q71.899 maps to 66 SNOMED CT concepts: 897274007, 773773006, 1003554003, 1145460003, 1145399007, and 61 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q71.899?

Q71.899 is linked to 1 UMLS Concept Unique Identifier: C2977508. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q71.899 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other reduction defects of unspecified upper limb 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 Q71.899?

There is no direct ICD-11 mapping available for Q71.899 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try Free View API Docs

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.