Status: current, Sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4946208017 | Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4946209013 | Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4946210015 | Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4946211016 | Autosomal dominant congenital fiber-type disproportion myopathy due to SELENON mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4946212011 | Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Is a | Congenital fiber-type disproportion myopathy due to selenoprotein N mutation | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR