Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303839018 | Autosomal recessive dopa responsive dystonia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303840016 | Autosomal recessive dopa responsive dystonia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303841017 | Autosomal recessive Segawa syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3303842012 | Tyrosine hydroxylase deficient dopa responsive dystonia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4554514017 | Tyrosine hydroxylase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
748731000241118 | dystonie dopa-sensible autosomique récessive (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
918181000172113 | dystonie dopa-sensible autosomique récessive | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
977781000172115 | DYT5b - dystonie dopa-sensible autosomique récessive | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3303843019 | Autosomal recessive dopa responsive dystonia (DYT5b) is a very rare neurometabolic disorder with a spectrum of symptoms ranging from those seen in dopa responsive dystonia to progressive infantile encephalopathy. Disease presents in infancy (most frequently in the first year of life) with a progressive hypokinetic rigid syndrome, involuntary jerky movements, postural tremor, or gait disturbances that may fluctuate during the day and show good or excellent responsiveness to levodopa in most cases. DYT5b is caused by mutations in the tyrosine hydroxylase TH gene (11p15.5). Inherited in an autosomal recessive manner. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive dopa responsive dystonia (disorder) | interprète (attribut) | Movement (observable entity) | true | Inferred relationship | Some | 2 | |
Autosomal recessive dopa responsive dystonia (disorder) | est un(e) (attribut) | Autosomal recessive idiopathic familial dystonia | true | Inferred relationship | Some | ||
Autosomal recessive dopa responsive dystonia (disorder) | est un(e) (attribut) | Diurnal dystonia | true | Inferred relationship | Some | ||
Autosomal recessive dopa responsive dystonia (disorder) | localisation d'une constatation (attribut) | Extrapyramidal system structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets