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 |
| 3315199014 | Syndactyly type 4 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3315200012 | Syndactyly type 4 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3315201011 | Haas type syndactyly | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401974010 | A rare non-syndromic syndactyly characterized by complete bilateral cutaneous fusion of all fingers, frequently associated with polydactyly (usually involving six digits and six metacarpals). Phalanges may fuse as a conglomerate mass of bones. Feet are occasionally affected. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401975011 | A rare non-syndromic syndactyly characterised by complete bilateral cutaneous fusion of all fingers, frequently associated with polydactyly (usually involving six digits and six metacarpals). Phalanges may fuse as a conglomerate mass of bones. Feet are occasionally affected. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Syndactyly type 4 (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Syndactyly type 4 (disorder) | Is a | Syndactyly (disorder) | true | Inferred relationship | Some | ||
| Syndactyly type 4 (disorder) | Associated morphology | Congenital abnormal fusion | false | Inferred relationship | Some | 1 | |
| Syndactyly type 4 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Syndactyly type 4 (disorder) | Finding site | Digit structure | true | Inferred relationship | Some | 1 | |
| Syndactyly type 4 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Syndactyly type 4 (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Syndactyly type 4 (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