Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3663220015 | Isolated unilateral hemispheric cerebellar hypoplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
768651000241113 | hypoplasie isolée unilatérale des hémisphères cérébelleux (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
934341000172117 | hypoplasie isolée unilatérale des hémisphères cérébelleux | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | est un(e) (attribut) | Finding of head region | true | Inferred relationship | Some | ||
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | morphologie associée (attribut) | Hypoplasia (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | localisation d'une constatation (attribut) | Cerebral hemisphere structure (body structure) | true | Inferred relationship | Some | 1 | |
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) | est un(e) (attribut) | Congenital hypoplasia of cerebrum | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets