Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3465122014 | Melhem Fahl syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3465123016 | Melhem Fahl syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3465124010 | Syndrome that was described in two siblings born to consanguineous parents in 1985 with the presence of 15 dorsal vertebrae and rib pairs. No other cases have been documented since the initial report. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5490541000241118 | syndrome des quinze vertèbres dorsales et quinze paires de côtes | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Melhem Fahl syndrome (disorder) | Is a | Dysostosis | true | Inferred relationship | Some | ||
| Melhem Fahl syndrome (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
| Melhem Fahl syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Melhem Fahl syndrome (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
| Melhem Fahl syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Melhem Fahl syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR