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 |
| 473704011 | Disorder with defective osteoid mineralisation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 730511011 | Disorder with defective osteoid mineralization (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 94570017 | Disorder with defective osteoid mineralization | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder with defective osteoid mineralisation | est un(e) (attribut) | maladie métabolique de l'os | true | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralisation | est un(e) (attribut) | troubles du métabolisme des minéraux (trouble) | true | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralisation | localisation d'une constatation (attribut) | Cartilaginous tissue structure | false | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralisation | localisation d'une constatation (attribut) | Structure of osteoid tissue (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal recessive hypophosphatemic bone disease | est un(e) (attribut) | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some | |
| rachitisme | est un(e) (attribut) | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some | |
| ostéomalacie | est un(e) (attribut) | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some | |
| Lipodystrophy, intellectual disability, deafness syndrome (disorder) | est un(e) (attribut) | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR