Status: current, Primitive. 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 | Active | Initial character case insensitive | SNOMED CT core |
| 3760269018 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 3760270017 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760271018 | Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760272013 | Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760276011 | Autosomal recessive secondary polycythemia non-Chuvash type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760277019 | Autosomal recessive secondary erythrocytosis non-Chuvash type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760278012 | Autosomal recessive secondary polycythaemia non-Chuvash type | en | Synonym | Active | Initial character case insensitive | 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 | Case sensitive | 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 | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Interprets | Red blood cell count | true | Inferred relationship | Some | 2 | |
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Is a | Familial erythrocytosis | true | Inferred relationship | Some | ||
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 | |
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Has interpretation | Above reference range | true | Inferred relationship | Some | 2 | |
| Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Interprets | Haematology procedure | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR