LD24.G1

ICD-11 MMS 2026-01

Crouzon disease

Description

Crouzon disease is a form of syndromic craniosynostosis characterised by craniosynostosis and facial hypoplasia.

Index terms

  • Crouzon disease
  • Vogt cephalosyndactyly

Exclusions from above levels

  • LD20.1 – Craniotelencephalic dysplasia
  • LD27.0Y – Sensenbrenner syndrome
  • LD28.0Y – Shprintzen-Goldberg craniosynostosis syndrome
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  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LD24.G0 – Pfeiffer syndrome
  • LD24.G2 – Apert syndrome
  • LD24.GY – Other specified syndromic craniosynostoses
  • LD24.GZ – Syndromic craniosynostoses, unspecified

Foundation entity

Crouzon disease – http://id.who.int/icd/entity/1535725821

Part of: LD24.G: Syndromic craniosynostoses › LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies