LD25.2

ICD-11 MMS 2026-01

Acrofacial dysostoses

Description

Any syndrome caused by failure of the face and limbs to correctly develop during the antenatal period.

Index terms

  • Acrofacial dysostoses
  • Acrofacial dysostosis, Nager type
  • Postaxial acrofacial dysostosis
Show allHide
  • Acrofacial dysostosis, Weyers type
  • Acrofacial dysostosis, Catania type
  • Acrofacial dysostosis, Rodriguez type
  • Acrofacial dysostosis, Palagonia type
  • Autosomal recessive acrofacial dysostosis
  • X-linked mandibulofacial dysostosis

Exclusions from above levels

  • LD26.4Y – Freeman-Sheldon syndrome
  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LD25.0 – Oromandibular-limb anomaly syndrome
  • LD25.1 – Fronto-otopalatodigital syndromes
  • LD25.3 – Craniofacial dysostoses
  • LD25.Y – Other specified syndromes with face or limb anomalies as a major feature
  • LD25.Z – Syndromes with face or limb anomalies as a major feature, unspecified

Foundation entity

Acrofacial dysostoses – http://id.who.int/icd/entity/1702160042

Part of: LD25: Syndromes with face or limb anomalies as a major feature › 20: Developmental anomalies