Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
315486012 | Fragile X chromosome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
591126013 | Fragile X chromosome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Fragile X syndrome | Is a | True | Fragile X chromosome | Inferred relationship | Some | |
FRAXF syndrome | Is a | True | Fragile X chromosome | Inferred relationship | Some | |
FRAXE intellectual disability syndrome | Is a | True | Fragile X chromosome | Inferred relationship | Some | |
Fragile X chromosome screening test | Has focus | True | Fragile X chromosome | Inferred relationship | Some | 3 |
FRAXA | Is a | True | Fragile X chromosome | Inferred relationship | Some | |
FRAXE | Is a | True | Fragile X chromosome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set