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 |
| 3700727014 | 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. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the VHL gene on chromosome 3p25. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3700728016 | 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. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the VHL gene on chromosome 3p25. | 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 |
This concept is not in any reference sets
FHIR