Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2025. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5447251010 | EDM7 - epiphyseal dysplasia multiple 7 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5447252015 | Multiple epiphyseal dysplasia type 7 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5447253013 | Multiple epiphyseal dysplasia type 7 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5447254019 | CANT1-related multiple epiphyseal dysplasia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5447255018 | MED7 - multiple epiphyseal dysplasia type 7 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5447264011 | A rare multiple epiphyseal dysplasia characterized by mild short stature, joint pain and early-onset osteoarthropathy, frequently requiring joint replacement. Radiographs from affected individuals may manifest features typical of Desbuquois dysplasia, including irregularly shaped capital femoral epiphyses, a short femoral neck (resembles the Swedish key appearance of the proximal femur) and advanced carpal ossification in the hands. However, some other features typical of Desbuquois dysplasia like joint dislocations, scoliosis, coronal clefts, or other hand anomalies including accessory ossification centers and/or delta phalanx are not observed. Anterior wedging of vertebral bodies, small epiphyses at the knees with metaphyseal flare may be present. Patients have normal metacarpal and phalangeal lengths, no distinctive facies nor neurologic complications. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5447265012 | A rare multiple epiphyseal dysplasia characterised by mild short stature, joint pain and early-onset osteoarthropathy, frequently requiring joint replacement. Radiographs from affected individuals may manifest features typical of Desbuquois dysplasia, including irregularly shaped capital femoral epiphyses, a short femoral neck (resembles the Swedish key appearance of the proximal femur) and advanced carpal ossification in the hands. However, some other features typical of Desbuquois dysplasia like joint dislocations, scoliosis, coronal clefts, or other hand anomalies including accessory ossification centres and/or delta phalanx are not observed. Anterior wedging of vertebral bodies, small epiphyses at the knees with metaphyseal flare may be present. Patients have normal metacarpal and phalangeal lengths, no distinctive facies nor neurologic complications. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Multiple epiphyseal dysplasia type 7 (disorder) | Is a | Multiple epiphyseal dysplasia | true | Inferred relationship | Some | ||
| Multiple epiphyseal dysplasia type 7 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Multiple epiphyseal dysplasia type 7 (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Interprets | Height / growth measure | false | Inferred relationship | Some | 3 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Finding site | Structure of epiphysis | true | Inferred relationship | Some | 1 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Interprets | Body height (observable entity) | true | Inferred relationship | Some | 3 | |
| Multiple epiphyseal dysplasia type 7 (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)