LD25.3

ICD-11 MMS 2026-01

Craniofacial dysostoses

Description

Syndromes caused by abnormal development of skull and facial bones. They may present with acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, or hypoplastic maxilla. Non-syndromic craniosynostosis, which is predominantly sporadic, is coded elsewhere.

Index terms

  • Craniofacial dysostoses
  • Craniofacial dysostosis
  • Oculomaxillofacial dysostosis
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  • Frontofacionasal dysostosis
  • Frontonasal dysplasia
  • Acromelic frontonasal dysplasia
  • Toriello syndrome
  • Acrofrontofacionasal dysostosis
  • Richieri-Costa-Colletto syndrome
  • Familial osteodysplasia, Anderson type
  • Craniofrontonasal dysplasia
  • Gollop syndrome

Excludes

  • LB70.0 – Craniosynostosis
  • LD25.1 – Frontometaphyseal dysplasia
  • LD25.2 – Acrofacial dysostosis, Weyers type

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
  • LD25.2 – Acrofacial 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

Craniofacial dysostoses – http://id.who.int/icd/entity/2114373392

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