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 |
| 3315203014 | Syndactyly type 5 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3315204015 | Syndactyly type 5 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5401976012 | A rare non-syndromic syndactyly characterized by soft tissue syndactyly of the 3rd and 4th fingers and the 2nd and 3rd toes associated with metacarpal and metatarsal fusion of the 4th and 5th digits. Shortening of fused metacarpals, ulnar deviation of fingers, interdigital cleft, camptodactyly, short distal phalanges, and absent distal interphalangeal creases have also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401977015 | A rare non-syndromic syndactyly characterised by soft tissue syndactyly of the 3rd and 4th fingers and the 2nd and 3rd toes associated with metacarpal and metatarsal fusion of the 4th and 5th digits. Shortening of fused metacarpals, ulnar deviation of fingers, interdigital cleft, camptodactyly, short distal phalanges, and absent distal interphalangeal creases have also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Syndactyly type 5 (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Syndactyly type 5 (disorder) | Is a | Syndactyly (disorder) | true | Inferred relationship | Some | ||
| Syndactyly type 5 (disorder) | Associated morphology | Congenital abnormal fusion | false | Inferred relationship | Some | 1 | |
| Syndactyly type 5 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Syndactyly type 5 (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 1 | |
| Syndactyly type 5 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Syndactyly type 5 (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Syndactyly type 5 (disorder) | Associated morphology | Abnormally fused structure (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR