Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3307276010 | FRAXF syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 3307277018 | FRAXF syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| FRAXF syndrome | Is a | Fragile X chromosome | true | Inferred relationship | Existential restriction modifier | ||
| FRAXF syndrome | Associated morphology | Chromosomal morphology | true | Inferred relationship | Existential restriction modifier | 1 | |
| FRAXF syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| FRAXF syndrome | Finding site | Sex chromosome X | true | Inferred relationship | Existential restriction modifier | 1 | |
| FRAXF syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| FRAXF syndrome | Is a | Congenital malformation | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR