Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2995200014 | Actin accumulation myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 2995370010 | Nemaline myopathy 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995468019 | Actin accumulation myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995863016 | Congenital myopathy with excess thin filaments | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Actin accumulation myopathy | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Actin accumulation myopathy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Actin accumulation myopathy | Finding site | Structure of musculoskeletal system | false | Inferred relationship | Existential restriction modifier | 1 | |
| Actin accumulation myopathy | Is a | Nemaline myopathy, early onset type | true | Inferred relationship | Existential restriction modifier | ||
| Actin accumulation myopathy | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Actin accumulation myopathy | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Actin accumulation myopathy | Is a | Autosomal hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR