Diagnosis Code: Q73.8

Short Description: Other reduction defects of unspecified limb(s)

Long Description: Other reduction defects of unspecified limb(s)

The code Q73.8 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
    • Reduction defects of unspecified limb (Q73)
      • Q73.8 Other reduction defects of unspecified limb(s)

Code Version: 2022 ICD-10-CM

Synonyms

• 10q partial trisomy syndrome
• Adactyly
• Ankylosis of joint of hand
• Aphalangy and syndactyly with microcephaly syndrome
• Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
• Brachydactyly and distal symphalangism syndrome
• Brachydactyly syndrome type B
• Brachydactyly syndrome type B
• Brachydactyly type A2
• Brachydactyly with syndactyly Zhao type
• Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
• Brachydactyly, short stature, retinitis pigmentosa syndrome
• Brachymesophalangia
• Brachymesophalangia
• Coloboma of macula with brachydactyly type B syndrome
• Congenital anomaly of macula
• Congenital coloboma of macula lutea
• Congenital hypoplasia of breast
• Congenital microgastria
• Congenital microgastria with limb reduction defect syndrome
• Cono-spondylar dysplasia
• Craniomicromelic syndrome
• Distal interphalangeal joint symphalangism
• Distal limb deficiency with micrognathia syndrome
• Dysraphism, cleft lip and palate, limb reduction defect syndrome
• Ectromelia
• Exostosis, anetoderma, brachydactyly type E syndrome
• Heart defect and limb shortening syndrome
• Ichthyosis, short stature, brachydactyly, microspherophakia syndrome
• Lentiglobus
• Liebenberg syndrome
• Limb mammary syndrome
• Longitudinal deficiency of limb
• Longitudinal deficiency of part of limb
• Mesoaxial synostotic syndactyly with phalangeal reduction syndrome
• Mesomelic dysplasia of upper limb
• Microlissencephaly micromelia syndrome
• Micromelia
• Micromelia
• Micromelic dwarfism Fryn type
• Microphakia
• Microspherophakia
• Oral-facial-digital syndrome with short stature and brachymesophalangia
• Partial trisomy of chromosome 10
• Robin sequence
• Robin sequence and oligodactyly syndrome
• Rudimentary digit
• Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome
• Skeletal dysplasia brachydactyly syndrome
• Spherophakia
• Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
• Symbrachydactyly
• Symphalangism
• Temtamy preaxial brachydactyly syndrome
• Thumb stiffness, brachydactyly, intellectual disability syndrome
• Trisomy 10
• Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome

Diagnostic Related Group(s)

The code Q73.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
• Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
• Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

References to Index of Diseases and Injuries

The code Q73.8 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Longitudinal reduction deformity of unspecified limb(s)
  • Ectromelia of limb NOS
  • Hemimelia of limb NOS
  • Reduction defect of limb NOS

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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