LD2F.1

ICD-11 MMS 2026-01

Syndromes with multiple structural anomalies, not of environmental origin

Exclusions from above levels

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

Child 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.16 – Otomandibular dysplasia
  • 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 children elsewhere

  • 5C60.0 – Oculocerebrorenal syndrome
  • LD2H.0 – Fraser syndrome
  • LD2H.3 – Waardenburg-Shah syndrome

Sibling codes

  • LD2F.0 – Toxic or drug-related embryofetopathies
  • LD2F.Y – Other specified syndromes with multiple structural anomalies, without predominant body system involvement
  • LD2F.Z – Syndromes with multiple structural anomalies, without predominant body system involvement, unspecified

Foundation entity

Syndromes with multiple structural anomalies, not of environmental origin – http://id.who.int/icd/entity/1106405864

Part of: LD2F: Syndromes with multiple structural anomalies, without predominant body system involvement › 20: Developmental anomalies