Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3766866013 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3766867016 | Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3766868014 | Lissencephaly with cerebellar hypoplasia type A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3766869018 | A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. | en | Definition | Active | Case sensitive | SNOMED CT core |
3777424013 | A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical grey matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | Is a | Lissencephaly with cerebellar hypoplasia | true | Inferred relationship | Some | ||
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | Is a | Genetic disease | false | Inferred relationship | Some | ||
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set