Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303317014 | Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303318016 | Aplasia of lacrimal and salivary gland | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6579091000146114 | aplasie van traan- en speekselklieren | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6970321000146114 | congenitale aplasie van traanklier gelijktijdig met congenitale aplasie van speekselklier (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6970331000146111 | congenitale aplasie van traanklier gelijktijdig met congenitale aplasie van speekselklier | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Congenital anomaly of lacrimal gland | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Congenital anomaly of salivary gland | false | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 2 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Associated morphology | Aplasia | false | Inferred relationship | Some | 3 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Finding site | Salivary gland structure (body structure) | true | Inferred relationship | Some | 2 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Finding site | Lacrimal gland structure | false | Inferred relationship | Some | 3 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Congenital aplasia of lacrimal structure (disorder) | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Finding site | Lacrimal gland structure | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Congenital partial absence of alimentary tract | false | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder) | Is a | Congenital absence of salivary gland | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets