Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302711017 | Congenital pontocerebellar hypoplasia type 2 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3302712012 | Congenital pontocerebellar hypoplasia type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3302713019 | PCH2 - pontocerebellar hypoplasia type 2 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3302714013 | Pontocerebellar hypoplasia type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3302715014 | The most common subtype of pontocerebellar hypoplasia with features of neonatal onset, lack of voluntary motor development and later progressive microencephaly, general clonus, development of chorea and spasticity.The majority of patients will not reach puberty. Inherited in an autosomal recessive manner. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital pontocerebellar hypoplasia type 2 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 2 | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 2 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 2 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 2 | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 2 | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 2 | Is a | Congenital pontocerebellar hypoplasia | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 2 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 2 | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 2 | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 2 | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 2 | Associated morphology | Hypoplasia | false | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 2 | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 2 | Finding site | Pontine structure | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 2 | 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