Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
38517016 | Chondrodysplasia punctata, Conradi-Hünermann type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
38518014 | Conradi-Hünermann syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
38519018 | Conradi's syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
38520012 | Chondrodysplasia punctata, Conradi-Hunermann type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
38521011 | Conradi-Hunermann syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
481474011 | Chondrodysplasia punctata, X-linked dominant type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
481475012 | Chondrodysplasia calcificans congenita | en | Synonym | Active | Case insensitive | SNOMED CT core |
752396018 | Chondrodysplasia punctata, Conradi-Hünermann type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Chondrodysplasia punctata, Conradi-Hünermann type | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 | |
Chondrodysplasia punctata, Conradi-Hünermann type | Is a | Chondrodysplasia punctata | false | Inferred relationship | Some | ||
Chondrodysplasia punctata, Conradi-Hünermann type | Is a | Cutaneous syndrome with ichthyosis | false | Inferred relationship | Some | ||
Chondrodysplasia punctata, Conradi-Hünermann type | Is a | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
Chondrodysplasia punctata, Conradi-Hünermann type | Occurrence | Congenital | false | Inferred relationship | Some | ||
Chondrodysplasia punctata, Conradi-Hünermann type | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
Chondrodysplasia punctata, Conradi-Hünermann type | Finding site | Structure of skin region | false | Inferred relationship | Some | ||
Chondrodysplasia punctata, Conradi-Hünermann type | Associated morphology | Dysplasia | false | Inferred relationship | Some | 1 | |
Chondrodysplasia punctata, Conradi-Hünermann type | Finding site | Skeletal system structure | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set