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 |
359705015 | Lipid storage myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
629192012 | Lipid storage myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lipid storage myopathy | Is a | Metabolic myopathy | true | Inferred relationship | Existential restriction modifier | ||
Lipid storage myopathy | Is a | Congenital anomaly of skeletal muscle | false | Inferred relationship | Existential restriction modifier | ||
Lipid storage myopathy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier | ||
Lipid storage myopathy | Is a | Lipid storage disease | true | Inferred relationship | Existential restriction modifier | ||
Lipid storage myopathy | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Lipid storage myopathy | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Neutral lipid storage disease with myopathy | Is a | True | Lipid storage myopathy | Inferred relationship | Existential restriction modifier | |
Genetic recurrent myoglobinuria | Is a | True | Lipid storage myopathy | Inferred relationship | Existential restriction modifier | |
Autosomal dominant myoglobinuria | Is a | True | Lipid storage myopathy | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets