Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3700721010 | Chuvash polycythemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3700722015 | Chuvash polycythaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3700723013 | Chuvash erythrocytosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3700724019 | Von Hippel Lindau dependent polycythaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3700725018 | Von Hippel Lindau dependent polycythemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3700726017 | Chuvash erythrocytosis (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404774017 | Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404775016 | Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythaemia disorder characterised by increased haemoglobin, haematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnoea and/or plethora. Patients present an increased risk of haemorrhage, thrombosis and early death. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Chuvash erythrocytosis | Interprets | Hematology procedure | true | Inferred relationship | Some | 3 | |
| Chuvash erythrocytosis | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Chuvash erythrocytosis | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Chuvash erythrocytosis | Is a | Familial erythrocytosis | true | Inferred relationship | Some | ||
| Chuvash erythrocytosis | Interprets | Red blood cell count | true | Inferred relationship | Some | 1 | |
| Chuvash erythrocytosis | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Chuvash erythrocytosis | Finding site | Erythrocyte | true | Inferred relationship | Some | 2 | |
| Chuvash erythrocytosis | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR