LD25.0

ICD-11 MMS 2026-01

Oromandibular-limb anomaly syndrome

Description

A syndrome caused by failure of the face and limbs to correctly develop during the antenatal period. This syndrome is characterised by malformations of the tongue, mandible, and limbs.

Excludes

  • LD27.0Y – Ectrodactyly - ectodermal dysplasia - cleft lip or palate
  • LD2F.1Y – Ectrodactyly - cleft palate

Exclusions from above levels

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

Child codes

  • LD25.00 – Oral-facial-digital syndrome
  • LD25.0Y – Other specified oromandibular-limb anomaly syndrome
  • LD25.0Z – Oromandibular-limb anomaly syndrome, unspecified

Sibling codes

  • LD25.1 – Fronto-otopalatodigital syndromes
  • LD25.2 – Acrofacial dysostoses
  • 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

Oromandibular-limb anomaly syndrome – http://id.who.int/icd/entity/1868700139

Allowed postcoordination axes

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