Status: current, 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 |
482352016 | Hereditary disorder of musculoskeletal system | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
755010013 | Hereditary disorder of musculoskeletal system (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2233501000172112 | myopathie héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
12732721000172112 | affection héréditaire du système musculosquelettique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
2233511000172110 | hereditaire myopathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary disorder of musculoskeletal system | Is a | Disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Hereditary disorder of musculoskeletal system | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
Hereditary disorder of musculoskeletal system | Finding site | Structure of musculoskeletal system (body structure) | true | Inferred relationship | Some | 1 |
Reference Sets
Belgian GP subset (foundation metadata concept)
Description inactivation indicator reference set