Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3703531018 | Huntington disease-like 3 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3703532013 | Huntington disease-like 3 (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
770031000241118 | maladie de Huntington-like 3 (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
882121000172115 | maladie de Huntington-like 3 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
964801000172116 | HDL3 - Huntington disease-like 3 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3703533015 | A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on brain MRI) progressive frontal cortical atrophy and bilateral caudate atrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Huntington disease-like 3 | interprète (attribut) | Movement (observable entity) | true | Inferred relationship | Some | 3 | |
Huntington disease-like 3 | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 1 | |
Huntington disease-like 3 | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Huntington disease-like 3 | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Huntington disease-like 3 | est un(e) (attribut) | Huntington disease-like syndrome | true | Inferred relationship | Some | ||
Huntington disease-like 3 | est un(e) (attribut) | Chronic brain syndrome | true | Inferred relationship | Some | ||
Huntington disease-like 3 | localisation d'une constatation (attribut) | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets