Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 88766016 | Hereditary myopathy associated with hydrocephalus | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 791500010 | Hereditary myopathy associated with hydrocephalus (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary myopathy associated with hydrocephalus | Is a | Myopathy | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary myopathy associated with hydrocephalus | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hereditary myopathy associated with hydrocephalus | Is a | Disorder of skeletal muscle | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary myopathy associated with hydrocephalus | Associated with | Hydrocephalus | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary myopathy associated with hydrocephalus | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR