Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303808015 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3303809011 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3303810018 | Lissencephaly with cerebellar hypoplasia type B | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3303811019 | A form of lissencephaly with cerebellar hypoplasia with main features of subtle microcephaly, hypotonia and neurological and cognitive development delay. Hippocampal malformation is a characteristic feature on imaging. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lissencephaly with cerebellar hypoplasia type B | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Lissencephaly with cerebellar hypoplasia type B | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Lissencephaly with cerebellar hypoplasia type B | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Lissencephaly with cerebellar hypoplasia type B | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Lissencephaly with cerebellar hypoplasia type B | Is a | Lissencephaly with cerebellar hypoplasia | true | Inferred relationship | Some | ||
Lissencephaly with cerebellar hypoplasia type B | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 2 | |
Lissencephaly with cerebellar hypoplasia type B | Finding site | Brain structure | false | Inferred relationship | Some | 2 | |
Lissencephaly with cerebellar hypoplasia type B | Associated morphology | Hypoplasia | false | Inferred relationship | Some | 3 | |
Lissencephaly with cerebellar hypoplasia type B | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Lissencephaly with cerebellar hypoplasia type B | Finding site | Cerebellar structure | false | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set