Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 359705015 | Lipid storage myopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 629192012 | Lipid storage myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Lipid storage myopathy | localisation d'une constatation (attribut) | structure de muscle squelettique | true | Inferred relationship | Some | 2 | |
| Lipid storage myopathy | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Lipid storage myopathy | est un(e) (attribut) | myopathie d'origine métabolique (trouble) | true | Inferred relationship | Some | ||
| Lipid storage myopathy | est un(e) (attribut) | Congenital anomaly of skeletal muscle | false | Inferred relationship | Some | ||
| Lipid storage myopathy | est un(e) (attribut) | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
| Lipid storage myopathy | est un(e) (attribut) | maladie de surchage lipidique | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neutral lipid storage disease with myopathy (disorder) | est un(e) (attribut) | True | Lipid storage myopathy | Inferred relationship | Some | |
| Genetic recurrent myoglobinuria (disorder) | est un(e) (attribut) | True | Lipid storage myopathy | Inferred relationship | Some | |
| Autosomal dominant myoglobinuria (disorder) | est un(e) (attribut) | True | Lipid storage myopathy | Inferred relationship | Some |
This concept is not in any reference sets
FHIR