Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3760268014 | Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760269018 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760270017 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760271018 | Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760272013 | Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760276011 | Autosomal recessive secondary polycythemia non-Chuvash type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760277019 | Autosomal recessive secondary erythrocytosis non-Chuvash type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760278012 | Autosomal recessive secondary polycythaemia non-Chuvash type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3760279016 | A rare hereditary haematologic disease characterised by an increase in haemoglobin, haematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnoea. In some cases, thrombophlebitis and arthralgia have also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3760280018 | A rare hereditary hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Interprets | Red blood cell count | true | Inferred relationship | Some | 2 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Is a | Familial erythrocytosis | true | Inferred relationship | Some | ||
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Has interpretation | Above reference range | true | Inferred relationship | Some | 2 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | Interprets | Hematology procedure | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR