Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4576246016 | Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4576247013 | Gaucher disease with ophthalmoplegia and cardiovascular calcification | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4576864015 | Gaucher's disease type 3C | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4578433019 | Gaucher-like disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4578434013 | Cardiovascular Gaucher disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder) | Finding site | Structure of nervous system (body structure) | true | Inferred relationship | Some | 2 | |
| Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder) | Is a | Subacute neuronopathic Gaucher's disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR