Syndromes with cerebellar anomalies as a major feature

Child codes

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

Sibling codes

• LD20.1 – Syndromes with lissencephaly as a major feature
• LD20.2 – Syndromes with microcephaly as a major feature
• LD20.3 – Syndromes with holoprosencephaly as a major feature
• LD20.4 – Syndromes with brain calcifications as a major feature
• LD20.Y – Other specified syndromes with central nervous system anomalies as a major feature
• LD20.Z – Syndromes with central nervous system anomalies as a major feature, unspecified

Foundation entity

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

Allowed postcoordination axes

• specificAnatomy