Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3324398018 | Blindness, scoliosis, arachnodactyly syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3324399014 | Blindness, scoliosis, arachnodactyly syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Blindness, scoliosis, arachnodactyly syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Blindness, scoliosis, arachnodactyly syndrome | Is a | Blindness AND/OR vision impairment level | true | Inferred relationship | Existential restriction modifier | ||
| Blindness, scoliosis, arachnodactyly syndrome | Is a | Connective tissue hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Blindness, scoliosis, arachnodactyly syndrome | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
| Blindness, scoliosis, arachnodactyly syndrome | Finding site | Connective tissue structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Blindness, scoliosis, arachnodactyly syndrome | Finding site | Structure of visual system | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR