Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1017241000172118 | ataxie cérébelleuse non progressive avec déficience intellectuelle | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3424625017 | Non-progressive cerebellar ataxia with intellectual disability (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3424626016 | Non-progressive cerebellar ataxia with intellectual disability | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
759411000241114 | ataxie cérébelleuse non progressive avec déficience intellectuelle (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3424627013 | Disease with characteristics of the onset in infancy of cerebellar ataxia, neonatal hypotonia (in some), mild developmental delay and in later life intellectual disability. Less common features include dysarthria, dysmetria and dysmorphic facial features (long face, bulbous nose long philtrum, thick lower lip and pointed chin). Caused by heterozygous disruption of the CAMTA1 gene on chromosome 1p36. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
ataxie cérébelleuse non progressive avec déficience intellectuelle | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Cerebellar ataxia | true | Inferred relationship | Some | ||
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Mental retardation | false | Inferred relationship | Some | ||
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
ataxie cérébelleuse non progressive avec déficience intellectuelle | localisation d'une constatation (attribut) | structure cérébelleuse | true | Inferred relationship | Some | 1 | |
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Intellectual disability | true | Inferred relationship | Some | ||
ataxie cérébelleuse non progressive avec déficience intellectuelle | est un(e) (attribut) | Hereditary ataxia (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
Description inactivation indicator reference set