Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3318109015 | X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3318110013 | X-linked dominant chondrodysplasia Chassaing Lacombe type | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5402251018 | X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5402252013 | X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterised by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Is a | Chondrodysplasia (disorder) | true | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder) | Is a | X-linked dominant hereditary disease (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR