Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3307387017 | Multiple osteochondroma of long bone (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307388010 | Multiple osteochondroma of long bone | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307389019 | Multiple osteochondroma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307391010 | Bessel Hagen disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3307390011 | The development of two or more cartilage capped bony outgrowths of the long bones.Develop and increase in size in the first decade of life, ceasing to grow when the growth plates close at puberty. The number may vary significantly within and between families. The majority are asymptomatic and located in bones that develop from cartilage, especially the long bones of the extremities, predominantly around the knee. The most important complication is malignant transformation towards secondary peripheral chondrosarcoma. Germline mutations in EXT1 or EXT2, are found in almost 90% of patients. An autosomal dominant disorder. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 7742611000172114 | maladie de Bessel-Hagen | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7742621000172116 | ostéochondromatose multiple d'un os long | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 7742631000172118 | plusieurs ostéochondromes d'un os long | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4633711000172110 | multipele osteochondromen van pijpbeen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Multiple osteochondroma of long bone (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Multiple osteochondroma of long bone (disorder) | Is a | Osteochondroma of bone | true | Inferred relationship | Some | ||
| Multiple osteochondroma of long bone (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
| Multiple osteochondroma of long bone (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
| Multiple osteochondroma of long bone (disorder) | Associated morphology | Osteochondroma | true | Inferred relationship | Some | 1 | |
| Multiple osteochondroma of long bone (disorder) | Finding site | Structure of long bone | true | Inferred relationship | Some | 1 | |
| Multiple osteochondroma of long bone (disorder) | Is a | Mass of body region | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR