Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4695184016 | Childhood-onset nemaline myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4695185015 | Childhood-onset nemaline myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4695189014 | Mild nemaline myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Childhood-onset nemaline myopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Childhood-onset nemaline myopathy | Is a | Nemaline myopathy | true | Inferred relationship | Existential restriction modifier | ||
| Childhood-onset nemaline myopathy | Occurrence | Childhood | true | Inferred relationship | Existential restriction modifier | 1 | |
| Childhood-onset nemaline myopathy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Childhood-onset nemaline myopathy | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Childhood-onset nemaline myopathy | Is a | Chronic disease of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Childhood-onset nemaline myopathy | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR