Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
369147012 | Choroidal atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
637341014 | Choroidal atrophy (finding) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5048431000241111 | atrophie de la choroïde | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
563431000274110 | Atrophie der Choroidea | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
619571000274119 | Aderhautatrophie | 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 |
Choroidal atrophy | Is a | Choroid finding | true | Inferred relationship | Some | ||
Choroidal atrophy | Finding site | Choroidal structure | false | Inferred relationship | Some | ||
Choroidal atrophy | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
Choroidal atrophy | Finding site | Choroidal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Senile atrophy of choroid | Is a | True | Choroidal atrophy | Inferred relationship | Some | |
Choroideremia | Is a | False | Choroidal atrophy | Inferred relationship | Some | |
Chorioretinal atrophy | Is a | True | Choroidal atrophy | Inferred relationship | Some | |
Diffuse secondary choroid atrophy | Is a | True | Choroidal atrophy | Inferred relationship | Some | |
A rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails. | Is a | True | Choroidal atrophy | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set