LD2F.16

ICD-11 MMS 2026-01

Otomandibular dysplasia

Description

Any condition characterised by malformation of facial bones and muscles. These conditions may present with eyes that slant downward, sparse eyelashes, eyelid coloboma, hearing loss, underdeveloped or absent vertebrae, or cleft palate.

Index terms

  • Otomandibular dysplasia
  • Oculo-auriculo-vertebral spectrum with radial defects
  • Auriculo-condylar syndrome
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  • Goldenhar syndrome
  • Hemifacial microsomia
  • Mandibulofacial dysostosis
  • mandibulofacial dysostosis syndrome
  • Treacher-Collins syndrome
  • Franceschetti-Klein syndrome
  • Acrodysostosis
  • Acrodysostosis with multiple hormone resistance

Exclusions from above levels

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

Sibling codes

  • LD2F.10 – Prune belly syndrome
  • LD2F.11 – VATER association
  • LD2F.12 – Sirenomelia
  • LD2F.13 – Meckel-Gruber syndrome
  • LD2F.14 – MURCS association
  • LD2F.15 – Noonan syndrome
  • LD2F.1Y – Other specified syndromes with multiple structural anomalies, not of environmental origin
  • LD2F.1Z – Syndromes with multiple structural anomalies, not of environmental origin, unspecified

Foundation entity

Otomandibular dysplasia – http://id.who.int/icd/entity/424177015

Part of: LD2F.1: Syndromes with multiple structural anomalies, not of environmental origin › LD2F: Syndromes with multiple structural anomalies, without predominant body system involvement › 20: Developmental anomalies