Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3737626014 | Autosomal dominant prognathism of mandible (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3737627017 | Autosomal dominant prognathism of mandible | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3737628010 | Autosomal dominant mandibular prognathism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6210261000146116 | autosomaal dominante prognathie van onderkaak | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6210281000146112 | autosomaal dominante prognathie van mandibula | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6996151000146110 | autosomaal dominante mandibulaire prognathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
7016111000146116 | autosomaal dominante mandibulaire prognathie (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3737625013 | A rare genetic developmental defect during embryogenesis disorder with characteristics of abnormal forward projection of the mandible beyond the standard relation to the cranial base, with lower incisors often overlapping the upper incisors, that is inherited in an autosomal dominant manner. Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant prognathism of mandible (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible (disorder) | Is a | Congenital anomaly of mandible | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible (disorder) | Is a | Mandibular prognathism | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible (disorder) | Associated morphology | Protrusion | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible (disorder) | Finding site | Bone structure of mandible | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible (disorder) | Is a | Congenital prognathism | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets