Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3663218018 | Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3663220015 | Isolated unilateral hemispheric cerebellar hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3663219014 | A rare non-syndromic cerebellar malformation with characteristics of loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (normal cerebral hemispheres, fourth ventricle, pons, medulla and midbrain). Patients may be asymptomatic or may present developmental and speech delay, hypotonia, abnormal ocular movements, persistent headaches and/or peripheral vertigo and ataxia. Neurological examination is otherwise normal. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Isolated unilateral hemispheric cerebellar hypoplasia | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia | Is a | Finding of head region | true | Inferred relationship | Some | ||
Isolated unilateral hemispheric cerebellar hypoplasia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia | Finding site | Cerebral hemisphere structure | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia | Is a | Congenital hypoplasia of cerebrum | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set