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 |
| 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 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Mandibuloacral dysplasia associated to MTX2 | Is a | True | Hereditary disorder of musculoskeletal system | Inferred relationship | Some | |
| Primary triglyceride deposit cardiomyovasculopathy (disorder) | Is a | True | Hereditary disorder of musculoskeletal system | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set
FHIR