Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3638199012 | Congenital temporomandibular joint ankylosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638200010 | Congenital ankylosis of temporomandibular joint (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638201014 | Congenital trismus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638202019 | Congenital ankylosis of temporomandibular joint | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 7426901000146119 | congenitale ankylose van kaakgewricht | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 7426911000146117 | congenitale ankylose van articulatio temporomandibularis | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 7426921000146110 | congenitale ankylose van kaakgewricht (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3638203012 | A rare maxillofacial disorder with characteristics of significant reduction in mouth opening in the absence of acquired factors (e.g. trauma, infection) contributing to the ankylosis. It is associated with variable degrees of facial dysmorphism (i.e. lateral deviation of the mandible and chin, lower facial asymmetry, retrognathia, micrognathia, dental malocclusion) and patients typically present with feeding and breathing difficulties. Developmental delay, hypotonia, seizures, and additional dysmorphic features (e.g. pectus excavatum, low-set ears, hypoplastic alae nasi) have also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital ankylosis of temporomandibular joint (disorder) | Is a | Ankylosis of temporomandibular joint (disorder) | true | Inferred relationship | Some | ||
| Congenital ankylosis of temporomandibular joint (disorder) | Is a | Congenital anomaly of joint | true | Inferred relationship | Some | ||
| Congenital ankylosis of temporomandibular joint (disorder) | Is a | Congenital anomaly of jaw | true | Inferred relationship | Some | ||
| Congenital ankylosis of temporomandibular joint (disorder) | Is a | Abnormal form of temporomandibular joint fossa | true | Inferred relationship | Some | ||
| Congenital ankylosis of temporomandibular joint (disorder) | Associated morphology | congenitale ankylose | false | Inferred relationship | Some | 1 | |
| Congenital ankylosis of temporomandibular joint (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital ankylosis of temporomandibular joint (disorder) | Finding site | Temporomandibular joint structure | true | Inferred relationship | Some | 1 | |
| Congenital ankylosis of temporomandibular joint (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital ankylosis of temporomandibular joint (disorder) | Associated morphology | Ankylosis | true | Inferred relationship | Some | 1 | |
| Congenital ankylosis of temporomandibular joint (disorder) | Is a | Congenital anomaly of face (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR