LD2F.1ICD-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 syndromeLD2F.11– VATER associationLD2F.12– SirenomeliaLD2F.13– Meckel-Gruber syndromeLD2F.14– MURCS associationLD2F.15– Noonan syndromeLD2F.16– Otomandibular dysplasiaLD2F.1Y– Other specified syndromes with multiple structural anomalies, not of environmental originLD2F.1Z– Syndromes with multiple structural anomalies, not of environmental origin, unspecified
Foundation children elsewhere
Sibling codes
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