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 | 
| 3315203014 | Syndactyly type 5 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 3315204015 | Syndactyly type 5 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Syndactyly type 5 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Syndactyly type 5 | Is a | Syndactyly | true | Inferred relationship | Existential restriction modifier | ||
| Syndactyly type 5 | Associated morphology | Congenital abnormal fusion | true | Inferred relationship | Existential restriction modifier | 1 | |
| Syndactyly type 5 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Syndactyly type 5 | Finding site | Digit structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Syndactyly type 5 | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Syndactyly type 5 | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets