Status: current, Defined. 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 | Case insensitive | SNOMED CT core |
3737627017 | Autosomal dominant prognathism of mandible | en | Synonym | Active | Case insensitive | SNOMED CT core |
3737628010 | Autosomal dominant mandibular prognathism | en | Synonym | Active | Case insensitive | SNOMED CT core |
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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant prognathism of mandible | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible | Is a | Congenital anomaly of mandible | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible | Is a | Mandibular prognathism | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible | Associated morphology | Protrusion | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible | Finding site | Bone structure of mandible | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant prognathism of mandible | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible | Is a | Congenital prognathism | true | Inferred relationship | Some | ||
Autosomal dominant prognathism of mandible | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set