LD20.ZICD-11 MMS 2026-01
Syndromes with central nervous system anomalies as a major feature, unspecified
Exclusions from above levels
LD2F.13– Meckel syndrome- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LD20.0– Syndromes with cerebellar anomalies as a major featureLD20.1– Syndromes with lissencephaly as a major featureLD20.2– Syndromes with microcephaly as a major featureLD20.3– Syndromes with holoprosencephaly as a major featureLD20.4– Syndromes with brain calcifications as a major featureLD20.Y– Other specified syndromes with central nervous system anomalies as a major feature
Foundation entity
Syndromes with central nervous system anomalies as a major feature – http://id.who.int/icd/entity/1800958996
Part of: LD20: Syndromes with central nervous system anomalies as a major feature › 20: Developmental anomalies