LD24.GZ

ICD-11 MMS 2026-01

Syndromic craniosynostoses, unspecified

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.G1 – Crouzon disease
LD24.G2 – Apert syndrome
LD24.GY – Other specified syndromic craniosynostoses

Foundation entity

Syndromic craniosynostoses – http://id.who.int/icd/entity/1908604930

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