Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 473704011 | Disorder with defective osteoid mineralisation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 730511011 | Disorder with defective osteoid mineralization (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 94570017 | Disorder with defective osteoid mineralization | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder with defective osteoid mineralisation | Is a | Metabolic bone disease | true | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralisation | Is a | Disorder of mineral metabolism | true | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralisation | Finding site | Cartilaginous tissue structure | false | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralisation | Finding site | Osteoid tissue | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal recessive hypophosphataemic bone disease | Is a | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some | |
| Rickets | Is a | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some | |
| Osteomalacia | Is a | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some | |
| Lipodystrophy, intellectual disability, deafness syndrome | Is a | True | Disorder with defective osteoid mineralisation | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
REPLACED BY association reference set
FHIR