Atrophoderma maculatum
Brachydactyly, short stature, retinitis pigmentosa syndrome
Congenital hypoplasia of bone of limb
Hemimelia
Exostosis, anetoderma, brachydactyly type E syndrome
Aplasia of bone of limb
Limb part reduction defect
Micromelus
Cardioskeletal syndrome Kuwaiti type
Skeletal dysplasia brachydactyly syndrome
Brachydactyly syndrome type B
Bork syndrome
Brachymesophalangia
Partial trisomy of chromosome 10
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome
Piussan Lenaerts Mathieu syndrome
Aphalangy and syndactyly with microcephaly syndrome
Duplication of chromosome 10
Micromelic dwarf
Syndactyly type 9
Anetoderma
Aplasia of limb
Coloboma of macula with brachydactyly type B syndrome
Congenital hypoplasia of limb
Limb reduction deformity
10q partial trisomy syndrome
Temtamy preaxial brachydactyly syndrome
Oral-facial-digital syndrome with short stature and brachymesophalangia
Congenital anomaly of macula
Congenital gastric hypoplasia
Brachydactyly type A2
OFD18 - oral-facial-digital syndrome type 18
Rudimentary digit
Aplasia of bone of extremity
Congenital hypoplasia of extremity
Abnormally short digit
Mononen Karnes Senac syndrome
Sillence syndrome
Sorsby syndrome
Aplasia of bone structure of extremity
Congenital dysplasia of radius
Robin sequence
Robin sequence and oligodactyly syndrome
Congenital spherophakia
Trisomy 10
Brachydactyly elbow wrist dysplasia
Tricho-retino-dento-digital syndrome
Mesomelic dysplasia of upper limb
Craniomicromelic syndrome
Brachydactyly Mohr Wriedt type
Lentiglobus
Hypoplasia of breast
Aplasia of extremity
Congenital coloboma of macula lutea
Microspherophakia
Stratton Garcia Young syndrome
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
Limb reduction defect
Pierre Robin sequence, oligodactyly syndrome
Hypoplastic breast
Exostosis, anetodermia, brachydactyly type E syndrome
defects limb reduction
Congenital microgastria with limb reduction defect syndrome
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
Longitudinal reduction deformity of unspecified limb(s)
Distal limb deficiency with micrognathia syndrome
Brachydactyly and distal symphalangism syndrome
Longitudinal deficiency of limb
Microgastria
15q26.3 microdeletion syndrome
Rhizomelic dysplasia
defect limbs reduction
Spherophakia
Longitudinal deficiency of part of limb
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
Congenital small lens
Coloboma of macula
Thumb stiffness, brachydactyly, intellectual disability syndrome
Hemimelia of limb NOS
Syndactyly Malik Percin type
Brachydactyly with joint dysplasia
Brachydactyly with syndactyly Zhao type
Micromelic dwarfism Fryn type
Pierre Robin association
Ectromelia
Limb mammary syndrome
Congenital microgastria
Distal interphalangeal joint symphalangism
Microlissencephaly micromelia syndrome
Dysraphism, cleft lip and palate, limb reduction defect syndrome
Shortened digit
Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome
Short stature, kyphosis, hypoplasia of basal ilia-cone epiphyses, facial dysmorphism syndrome
Basel Vanagaite Sirota syndrome
Micromelia
Liebenberg syndrome
Symbrachydactyly
10q24 microduplication syndrome
Ectromelia of limb NOS
Orofaciodigital syndrome type 18
Medeira Dennis Donnai syndrome
Johnson Munson syndrome
Reduction deformity of limb
Heart defect and limb shortening syndrome
Buttiens Fryns syndrome
Reduction defect of limb NOS
Adactyly
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome
Congenital small stomach
Mesoaxial synostotic syndactyly with phalangeal reduction syndrome
Pierre Robin syndrome
Micrognathia-glossoptosis syndrome
Nanomelia
Longitudinal deficiency of limb (disorder)
Congenital hypoplasia of breast
Microphakia
Congenital hypoplasia of bone of extremity
Reduction deformity of part of limb
Cono-spondylar dysplasia

Frequently Asked Questions

What is the ICD-10 code for other reduction defects of unspecified limb(s)?

The ICD-10-CM code for other reduction defects of unspecified limb(s) is Q73.8. The full clinical description is "Other reduction defects of unspecified limb(s)". Q73.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q73.8 mean?

ICD-10-CM code Q73.8 represents “Other reduction defects of unspecified limb(s)”. 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 Q73.8 a billable code?

Yes, Q73.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q73.8 in?

Q73.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q73.8 map to?

Q73.8 maps to 60 SNOMED CT concepts: 73035005, 722429003, 783551005, 897331007, 275348004, and 55 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q73.8?

Q73.8 is linked to 4 UMLS Concept Unique Identifiers: C2910323, C0265547, C2910324, C0478069. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q73.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other reduction defects of unspecified limb(s) 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 Q73.8?

Q73.8 maps to the ICD-11 code: LD24.0Z (Syndromes with micromelia, 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.