Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
29310019 | Hereditary pure erythrocytosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
29313017 | Familial polycythemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
29315012 | Familial erythrocytosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
478114012 | Familial polycythaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
744529012 | Familial erythrocytosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial erythrocytosis due to diphosphoglycerate mutase deficiency | Is a | True | Familial erythrocytosis | Inferred relationship | Existential restriction modifier | |
Familial polycythemia vera | Is a | True | Familial erythrocytosis | Inferred relationship | Existential restriction modifier | |
High oxygen affinity hemoglobin polycythemia | Is a | True | Familial erythrocytosis | Inferred relationship | Existential restriction modifier | |
Chuvash erythrocytosis | Is a | True | Familial erythrocytosis | Inferred relationship | Existential restriction modifier | |
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Is a | True | Familial erythrocytosis | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets