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 |
| 94570017 | Disorder with defective osteoid mineralization | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 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 |
| 2080821000005113 | Sygdom med mangelfuld osteoid mineralisering | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Disorder with defective osteoid mineralization | Is a | Metabolic bone disease | true | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralization | Is a | Disorder of mineral metabolism | true | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralization | Finding site | struktur af bruskvæv | false | Inferred relationship | Some | ||
| Disorder with defective osteoid mineralization | Finding site | Osteoid tissue | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Rickets | Is a | True | Disorder with defective osteoid mineralization | Inferred relationship | Some | |
| Osteomalacia | Is a | True | Disorder with defective osteoid mineralization | Inferred relationship | Some | |
| Autosomal recessive hypophosphatemic bone disease | Is a | True | Disorder with defective osteoid mineralization | Inferred relationship | Some | |
| A rare form of genetic lipodystrophy, reported in 3 patients from one family to date, characterized by generalized congenital lipodystrophy, low birth weight, progressive sensorineural deafness occurring in childhood, intellectual deficit, progressive osteopenia, delayed skeletal maturation, skeletal abnormalities described as slender, undermineralized tubular bones, and dense metaphyseal striations in the distal femur, ulna and radius of older patients. Autosomal recessive inheritance has been suggested. | Is a | True | Disorder with defective osteoid mineralization | Inferred relationship | Some |
This concept is not in any reference sets
FHIR