Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3324398018 | Blindness, scoliosis, arachnodactyly syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3324399014 | Blindness, scoliosis, arachnodactyly syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401639011 | This syndrome associates progressive visual loss with scoliosis or kyphoscoliosis and arachnodactyly of the fingers and toes. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Blindness, scoliosis, arachnodactyly syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Blindness, scoliosis, arachnodactyly syndrome (disorder) | Is a | Blindness AND/OR vision impairment level | true | Inferred relationship | Some | ||
Blindness, scoliosis, arachnodactyly syndrome (disorder) | Is a | Connective tissue hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Blindness, scoliosis, arachnodactyly syndrome (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Blindness, scoliosis, arachnodactyly syndrome (disorder) | Finding site | Connective tissue structure | true | Inferred relationship | Some | 1 | |
Blindness, scoliosis, arachnodactyly syndrome (disorder) | Finding site | Structure of visual system (body structure) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)