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FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR Version n/a
User: [n/a]
Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2023. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2640894017 | Corneal thinning (finding) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2644963011 | Corneal thinning | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2648787014 | Thin cornea | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5874621000241117 | amincissement cornéen | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 5874631000241115 | amincissement de la cornée | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Corneal thinning (finding) | Is a | Corneal finding (finding) | true | Inferred relationship | Some | ||
| Corneal thinning (finding) | Finding site | Corneal structure | false | Inferred relationship | Some | 1 | |
| Corneal thinning (finding) | Is a | Clinical finding (finding) | false | Inferred relationship | Some | ||
| Corneal thinning (finding) | Has interpretation | Thin | true | Inferred relationship | Some | 1 | |
| Corneal thinning (finding) | Interprets | Corneal thickness (observable entity) | true | Inferred relationship | Some | 1 | |
| Corneal thinning (finding) | Is a | Eye measurements - finding | true | Inferred relationship | Some | ||
| Corneal thinning (finding) | Finding site | Corneal structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital keratoglobus | Due to | False | Corneal thinning (finding) | Inferred relationship | Some | 2 |
| A rare, hereditary connective tissue disease characterized by severe ocular manifestations due to extreme corneal thinning and fragility with rupture in the absence of significant trauma, often leading to irreversible blindness. Extraocular manifestations comprise deafness, developmental hip dysplasia, and joint hypermobility. | Is a | True | Corneal thinning (finding) | Inferred relationship | Some | |
| Keratoglobus (disorder) | Is a | True | Corneal thinning (finding) | Inferred relationship | Some | |
| Pellucid marginal corneal degeneration | Is a | True | Corneal thinning (finding) | Inferred relationship | Some |
This concept is not in any reference sets