Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 496572011 | Adenosine deaminase superactivity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2913809012 | Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2915153015 | Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3780603016 | Hereditary nonspherocytic haemolytic anaemia due to increased adenosine deaminase activity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5159269019 | Hemolytic anemia due to erythrocyte adenosine deaminase overproduction | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5159270018 | Haemolytic anaemia due to erythrocyte adenosine deaminase overproduction | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5159271019 | HNSHA (hereditary nonspherocytic hemolytic anemia) due to increased adenosine deaminase activity | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5159273016 | HNSHA (hereditary nonspherocytic haemolytic anaemia) due to increased adenosine deaminase activity | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5159274010 | A rare genetic haematologic disease characterised by mild chronic haemolytic anaemia (due to highly elevated adenosine deaminase activity in red blood cells resulting in their premature destruction), elevated reticulocyte count, splenomegaly and mild hyperbilirubinaemia. Other cells and tissues are not affected. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5159275011 | A rare genetic hematologic disease characterized by mild chronic hemolytic anemia (due to highly elevated adenosine deaminase activity in red blood cells resulting in their premature destruction), elevated reticulocyte count, splenomegaly and mild hyperbilirubinemia. Other cells and tissues are not affected. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Is a | Erythrocyte enzyme deficiency | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Some | 4 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Is a | Hereditary nonspherocytic haemolytic anaemia | true | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Has definitional manifestation | Hemolysis | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 1 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 1 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Interprets | Red blood cell count | true | Inferred relationship | Some | 2 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Interprets | Erythrocyte destruction | false | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Has interpretation | Present | true | Inferred relationship | Some | 3 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Interprets | Hemolysis (observable entity) | true | Inferred relationship | Some | 3 | |
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) | Is a | Disorder of purine metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR