LD26.1

ICD-11 MMS 2026-01

Complex brachydactylies

Description

A disease caused by failure of the digits to correctly develop during the antenatal period. This disease is characterised by multiple digits of below normal length. This condition may be associated with mutation in the GDF5 gene.

Index terms

  • Complex brachydactylies
  • Brachydactyly type A1
  • Brachydactyly type A2
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  • Brachydactyly type A3
  • Brachydactyly type A4
  • Brachydactyly type A5
  • Brachydactyly type A6
  • Brachydactyly type A7
  • Brachydactyly type B
  • Brachydactyly type B2
  • Brachydactyly type C
  • Brachydactyly type D
  • Brachydactyly type E
  • Ballard syndrome
  • Brachydactyly types B and E combined
  • Pitt-Williams brachydactyly
  • Brachydactyly-elbow wrist dysplasia

Excludes

Exclusions from above levels

  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LD26.0 – Combined reduction defects of upper and lower limbs
  • LD26.2 – Syndromes with limb duplication, polydactyly, syndactyly or triphalangism
  • LD26.3 – Syndromes with synostoses of limbs
  • LD26.4 – Arthrogryposis syndromes
  • LD26.5 – Constriction rings
  • LD26.6 – Congenital vascular bone syndromes
  • LD26.Y – Other specified syndromes with limb anomalies as a major feature
  • LD26.Z – Syndromes with limb anomalies as a major feature, unspecified

Foundation entity

Complex brachydactylies – http://id.who.int/icd/entity/1952945042

Allowed postcoordination axes

Part of: LD26: Syndromes with limb anomalies as a major feature › 20: Developmental anomalies