Syndromes with cerebellar 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

LD20.00 – Joubert syndrome
LD20.01 – Pontocerebellar hypoplasia
LD20.0Y – Other specified syndromes with cerebellar anomalies as a major feature

Foundation entity

Syndromes with cerebellar anomalies as a major feature – http://id.who.int/icd/entity/1488858760

Allowed postcoordination axes

specificAnatomy

Part of: LD20.0: Syndromes with cerebellar anomalies as a major feature › LD20: Syndromes with central nervous system anomalies as a major feature › 20: Developmental anomalies