Status: current, Defined. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303315018 | Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3303317014 | Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303318016 | Aplasia of lacrimal and salivary gland | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303320018 | A rare autosomal dominant disorder with features of aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying manifestations from infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set