Status: current, 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 |
3766870017 | Acquired hemophilia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766871018 | Acquired haemophilia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766872013 | Acquired hemophilia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766870017 | Acquired hemophilia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766871018 | Acquired haemophilia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766872013 | Acquired hemophilia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3766873015 | A rare hemorrhagic disorder due to an acquired coagulation factor defect characterized by sudden, spontaneous, and often severe bleeding, manifesting with skin, muscle and mucous membrane hemorrhages, in persons without a previous bleeding tendency. Additional symptoms may include epistaxis, gastrointestinal and/or urogenital bleeding, spontaneous bruising, melena and hematuria. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3766874014 | A rare haemorrhagic disorder due to an acquired coagulation factor defect characterised by sudden, spontaneous, and often severe bleeding, manifesting with skin, muscle and mucous membrane haemorrhages, in persons without a previous bleeding tendency. Additional symptoms may include epistaxis, gastrointestinal and/or urogenital bleeding, spontaneous bruising, melaena and haematuria. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
652171000274113 | Erworbene Hämophilie | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5592401000241112 | hémophilie acquise | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5592401000241112 | hémophilie acquise | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
652171000274113 | Erworbene Hämophilie | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3393261001000118 | Wachstumsverzögerung durch IGF-1-Resistenz | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acquired hemophilia | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Acquired hemophilia | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Acquired hemophilia | Is a | Acquired coagulation factor deficiency (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Acquired hemophilia | Is a | Haemophilia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Acquired hemophilia | Occurrence | Period of life between birth and death | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Acquired factor IX deficiency disease | Is a | True | Acquired hemophilia | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets