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 |
| 4945365014 | Autosomal dominant central core disease (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4945366010 | Autosomal dominant central core disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4945367018 | Autosomal dominant central core myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant central core disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant central core disease | Is a | Central core disease | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant central core disease | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant central core disease | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant central core disease | Associated morphology | Central cores | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant central core disease | 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