Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 53727015 | Congenital fiber type disproportion | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 53728013 | Congenital fiber type disproportion myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 485146017 | Congenital fibre type disproportion myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 763410017 | Congenital fiber type disproportion myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital fiber type disproportion myopathy | Is a | Congenital myopathy | false | Inferred relationship | Existential restriction modifier | ||
| Congenital fiber type disproportion myopathy | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | ||
| Congenital fiber type disproportion myopathy | Is a | Congenital anomaly of skeletal muscle | false | Inferred relationship | Existential restriction modifier | ||
| Congenital fiber type disproportion myopathy | Finding site | Skeletal muscle system structure | false | Inferred relationship | Existential restriction modifier | ||
| Congenital fiber type disproportion myopathy | Associated morphology | Congenital anomaly | false | Inferred relationship | Existential restriction modifier | ||
| Congenital fiber type disproportion myopathy | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR