Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3755561018 | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755562013 | Huntington disease-like syndrome due to C9ORF72 expansions | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755563015 | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755564014 | C9ORF72-related Huntington disease phenocopy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755565010 | A rare genetic neurodegenerative disease characterised by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioural problems. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755566011 | A rare genetic neurodegenerative disease characterized by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioral problems. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755561018 | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755562013 | Huntington disease-like syndrome due to C9ORF72 expansions | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755563015 | Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755564014 | C9ORF72-related Huntington disease phenocopy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755565010 | A rare genetic neurodegenerative disease characterised by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioural problems. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755566011 | A rare genetic neurodegenerative disease characterized by movement disorders, including dystonia, chorea, myoclonus, tremor and rigidity. Associated features are also cognitive and memory impairment, early psychiatric disturbances and behavioral problems. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3454661001000118 | Chorea Huntington-ähnliches Syndrom durch C9ORF72-Expansionen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6316821000241116 | syndrome de type maladie de Huntington dû à des expansions de C9ORF72 (chromosome 9 open reading frame 72) | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6316821000241116 | syndrome de type maladie de Huntington dû à des expansions de C9ORF72 (chromosome 9 open reading frame 72) | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3454661001000118 | Chorea Huntington-ähnliches Syndrom durch C9ORF72-Expansionen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets