Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3333166017 | Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4544148017 | Hemolytic uremic syndrome with either a family history of hemolytic uremic syndrome or a genetic mutation known to cause hemolytic uremic syndrome, or both. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3333162015 | Familial haemolytic uraemic syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3333164019 | Familial hemolytic uremic syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3333165018 | Familial hemolytic uremic syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6177871000241117 | SHU (syndrome hémolytique et urémique) familial | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6177881000241115 | syndrome hémolytique et urémique familial | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Is a | Familial disease | true | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Is a | Congenital hemolytic uremic syndrome (disorder) | false | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Occurrence | Congenital | false | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Clinical course | Sudden onset AND/OR short duration (qualifier value) | true | Inferred relationship | Some | 1 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Erythrocyte (cell) | false | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Kidney structure | true | Inferred relationship | Some | 7 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has definitional manifestation | érythropénie | false | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has definitional manifestation | Haemolysis | false | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has interpretation | Below reference range | true | Inferred relationship | Some | 10 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 10 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has interpretation | Below reference range | true | Inferred relationship | Some | 11 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Red blood cell count | true | Inferred relationship | Some | 11 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Associated morphology | Schistocyte | false | Inferred relationship | Some | 12 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | 12 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Erythrocyte destruction | false | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Is a | Hemolytic uremic syndrome | true | Inferred relationship | Some | ||
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Associated morphology | Schistocyte | true | Inferred relationship | Some | 4 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has interpretation | Below reference range | true | Inferred relationship | Some | 3 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Platelet count | true | Inferred relationship | Some | 3 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Measurement of renal function | false | Inferred relationship | Some | 2 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has interpretation | Impaired | false | Inferred relationship | Some | 2 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Hemolysis (observable entity) | true | Inferred relationship | Some | 5 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Erythrocyte (cell) | false | Inferred relationship | Some | 6 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has interpretation | Present (qualifier value) | true | Inferred relationship | Some | 5 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Occurrence | Any period of life commencing after birth, but before death. | false | Inferred relationship | Some | 6 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Erythrocyte (cell) | true | Inferred relationship | Some | 8 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Interprets | Renal function | true | Inferred relationship | Some | 9 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Has interpretation | Impaired | true | Inferred relationship | Some | 9 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Structure of capillary blood vessel | true | Inferred relationship | Some | 2 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Associated morphology | Microthrombus (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Finding site | Structure of arteriole | true | Inferred relationship | Some | 6 | |
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. | Associated morphology | Microthrombus (morphologic abnormality) | true | Inferred relationship | Some | 6 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets