Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
158711011 | Congenital deafness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
267831000172119 | surdité congénitale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
484491000241117 | surdité congénitale (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
840063013 | Congenital deafness (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Autosomal dominant aplasia and myelodysplasia (disorder) | est un(e) (attribut) | True | Congenital deafness | Inferred relationship | Some | |
Congenital prelingual deafness | est un(e) (attribut) | True | Congenital deafness | Inferred relationship | Some | |
Neutropenia, monocytopenia, deafness syndrome (disorder) | est un(e) (attribut) | True | Congenital deafness | Inferred relationship | Some | |
Deafness, vitiligo, achalasia syndrome | est un(e) (attribut) | True | Congenital deafness | Inferred relationship | Some | |
Congenital deafness with labyrinthine aplasia, microtia and microdontia | est un(e) (attribut) | True | Congenital deafness | Inferred relationship | Some | |
Sinoatrial node dysfunction and deafness | est un(e) (attribut) | True | Congenital deafness | Inferred relationship | Some |
Reference Sets