Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3760268014 | Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760269018 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760270017 | Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760271018 | Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760272013 | Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760276011 | Autosomal recessive secondary polycythemia non-Chuvash type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760277019 | Autosomal recessive secondary erythrocytosis non-Chuvash type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760278012 | Autosomal recessive secondary polycythaemia non-Chuvash type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Interprets | Red blood cell count | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Is a | Familial erythrocytosis | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Finding site | Erythrocyte | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene | Interprets | Hematology procedure | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR