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 |
3302210017 | Ehlers-Danlos syndrome classic type (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302211018 | Ehlers-Danlos syndrome classic type | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302212013 | Ehlers-Danlos syndrome classical type | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5255462018 | Classical Ehlers-Danlos syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302213015 | A form of Ehlers-Danlos syndrome that affects the soft connective tissue and is characterized by skin hyperextensibility, widened atrophic scars and joint hypermobility. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302214014 | A form of Ehlers-Danlos syndrome that affects the soft connective tissue and is characterised by skin hyperextensibility, widened atrophic scars and joint hypermobility. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Ehlers-Danlos syndrome, type 2 | Is a | False | Ehlers-Danlos syndrome classic type (disorder) | Inferred relationship | Some | |
Ehlers-Danlos syndrome, type 1 | Is a | False | Ehlers-Danlos syndrome classic type (disorder) | Inferred relationship | Some | |
Ehlers-Danlos syndrome classic type 2 | Is a | True | Ehlers-Danlos syndrome classic type (disorder) | Inferred relationship | Some |
This concept is not in any reference sets