Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3775348016 | Bifid nose (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3775349012 | Bifid nose | en | Synonym | Active | Case insensitive | SNOMED CT core |
3775350012 | Bifid nose is a rare congenital malformation of presumed autosomal dominant or recessive inheritance with characteristics of clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia while other malformations such as hypertelorbitism and midline clefts of the lip may also be associated. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
BNAR syndrome | Is a | True | Bifid nose | Inferred relationship | Some | |
Trigonocephaly with bifid nose and acral anomaly syndrome | Is a | True | Bifid nose | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set