Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3439079017 | Congenital aplasia of lacrimal structure (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3439080019 | Congenital aplasia of lacrimal structure | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5846051000241110 | aplasie congénitale d'une structure lacrymale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
535991000274113 | Kongenitale Aplasie des Apparatus lacrimalis | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
602801000274119 | Kongenitale Aplasie des Tränenapparats | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital aplasia of lacrimal structure (disorder) | Is a | Congenital anomaly of lacrimal system | true | Inferred relationship | Some | ||
Congenital aplasia of lacrimal structure (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal structure (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal structure (disorder) | Finding site | Lacrimal structure | true | Inferred relationship | Some | 1 | |
Congenital aplasia of lacrimal structure (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital absence of lacrimal drainage structure (disorder) | Is a | False | Congenital aplasia of lacrimal structure (disorder) | Inferred relationship | Some | |
A rare autosomal dominant disorder characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying features since infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation. | Is a | True | Congenital aplasia of lacrimal structure (disorder) | Inferred relationship | Some | |
Agenesis of nasolacrimal duct | Is a | True | Congenital aplasia of lacrimal structure (disorder) | Inferred relationship | Some | |
Agenesis of punctum lacrimale | Is a | True | Congenital aplasia of lacrimal structure (disorder) | Inferred relationship | Some | |
Congenital complete absence of nasolacrimal drainage system (disorder) | Is a | True | Congenital aplasia of lacrimal structure (disorder) | Inferred relationship | Some |
This concept is not in any reference sets