Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3755222010 | Congenital pseudoarthrosis of limb (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3755223017 | Congenital pseudoarthrosis of limb | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3755224011 | A rare genetic non-syndromic limb malformation with characteristics of delayed union or non-union of a long bone, resulting in formation of a false joint, with abnormal mobility and angulation at the pseudoarthrosis site, which manifests with progressive anterolateral forearm or leg bowing, limb shortening, and non-healing fractures. Typical histopathological findings include fibromatosis-like proliferation in the soft tissues with cystic or dysplastic lesions. Neurofibromatosis and osteofibrous dysplasia are frequently associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3755222010 | Congenital pseudoarthrosis of limb (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3755223017 | Congenital pseudoarthrosis of limb | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3755224011 | A rare genetic non-syndromic limb malformation with characteristics of delayed union or non-union of a long bone, resulting in formation of a false joint, with abnormal mobility and angulation at the pseudoarthrosis site, which manifests with progressive anterolateral forearm or leg bowing, limb shortening, and non-healing fractures. Typical histopathological findings include fibromatosis-like proliferation in the soft tissues with cystic or dysplastic lesions. Neurofibromatosis and osteofibrous dysplasia are frequently associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
1055121000195111 | Pseudoarthrose der Gliedmassen, kongenitale | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5906061000241113 | pseudoarthrose congénitale d'un membre | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5906061000241113 | pseudoarthrose congénitale d'un membre | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1055121000195111 | Pseudoarthrose der Gliedmassen, kongenitale | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3453421001000113 | Pseudoarthrose der Gliedmaßen, kongenitale | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital pseudoarthrosis of tibia (disorder) | Is a | True | Congenital pseudoarthrosis of limb (disorder) | Inferred relationship | Existential restriction modifier (core metadata concept) | |
Congenital pseudoarthrosis of clavicle (disorder) | Is a | True | Congenital pseudoarthrosis of limb (disorder) | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets