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 |
| 3008914013 | Cap myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3008979013 | Cap disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3009097013 | Congenital myopathy with caps | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3009579013 | Cap myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cap myopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cap myopathy | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Cap myopathy | Is a | Disorder of skeletal muscle | true | Inferred relationship | Existential restriction modifier | ||
| Cap myopathy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
| Cap myopathy | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Cap myopathy | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | ||
| Cap myopathy | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Cap myopathy | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR