Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3775387016 | Oligodontia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3775388014 | Selective tooth agenesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3775389018 | Oligodontia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3775390010 | Oligodontia is a rare developmental dental anomaly with clinical features that include six or more missing teeth, lack of development of maxillary and mandibular alveolar bone height and reduced lower facial height. Variation in tooth morphology is also observed along with problems in tooth development, eruption and exfoliation. Possible causes of oligodontia include viral disease during pregnancy, genetic predisposition, metabolic imbalances, developmental abnormalities and environmental factors. Autosomal dominant mutations in PAX9 and MSX1 have been found in patients with molar non-syndromic oligodontia. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
X-linked oligodontia | Is a | True | Oligodontia | Inferred relationship | Some | |
Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome | Is a | True | Oligodontia | Inferred relationship | Some | |
Oligodontia and cancer predisposition syndrome | Is a | True | Oligodontia | Inferred relationship | Some | |
Cleft palate with stapes fixation and oligodontia syndrome | Is a | True | Oligodontia | Inferred relationship | Some | |
Deafness and oligodontia syndrome | Is a | True | Oligodontia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set