LD24.9

ICD-11 MMS 2026-01

Acromesomelic dysplasias

Description

A group of rare disorders characterised by shortening of the bones of the forearms, lower legs, hands and feet.

Index terms

  • Acromesomelic dysplasias
  • Acromesomelic dysplasia, Maroteaux type
  • Acromesomelic dysplasia, Grebe type
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  • Acromesomelic dysplasia, Hunter-Thomson type
  • Verloes-David syndrome
  • 8q13 deletion
  • Mesomelia - synostoses
  • Mesomelia-synostoses syndrome
  • Monosomy 8q13

Excludes

Exclusions from above levels

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

Sibling codes

  • LD24.0 – Syndromes with micromelia
  • LD24.1 – Bone diseases with increased bone density
  • LD24.2 – Bone diseases with disorganised development of skeletal components
  • LD24.3 – Spondyloepiphyseal or spondyloepimetaphyseal dysplasias
  • LD24.4 – Spondylometaphyseal dysplasias
  • LD24.5 – Spondylodysplastic dysplasias
  • LD24.6 – Multiple epiphyseal dysplasia or pseudoachondroplasia
  • LD24.7 – Multiple metaphyseal dysplasias
  • LD24.8 – Acromelic dysplasias
  • LD24.A – Mesomelic or rhizomesomelic dysplasias
  • LD24.B – Short rib syndromes
  • LD24.C – Bent bone dysplasias
  • LD24.D – Slender bone dysplasias
  • LD24.E – Bone dysplasias with multiple joint dislocations
  • LD24.F – Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments
  • LD24.G – Syndromic craniosynostoses
  • LD24.H – Dysostoses with predominant vertebral and costal involvement
  • LD24.J – Patellar dysostoses
  • LD24.K – Genetic bone diseases with decreased bone density
  • LD24.Y – Other specified syndromes with skeletal anomalies as a major feature
  • LD24.Z – Syndromes with skeletal anomalies as a major feature, unspecified

Foundation entity

Acromesomelic dysplasias – http://id.who.int/icd/entity/2002361676

Part of: LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies