Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
29310019 | Hereditary pure erythrocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
29313017 | Familial polycythemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
29315012 | Familial erythrocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
478114012 | Familial polycythaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
744529012 | Familial erythrocytosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | Is a | True | Familial erythrocytosis | Inferred relationship | Some | |
Familial erythrocytosis due to diphosphoglycerate mutase deficiency | Is a | True | Familial erythrocytosis | Inferred relationship | Some | |
Familial polycythaemia vera | Is a | True | Familial erythrocytosis | Inferred relationship | Some | |
High oxygen affinity haemoglobin polycythaemia | Is a | True | Familial erythrocytosis | Inferred relationship | Some | |
Chuvash erythrocytosis | Is a | True | Familial erythrocytosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set