Status: current, Defined. Date: 31-Jan 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
124062010 | Pyruvate kinase deficiency anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
200479013 | Pyruvate kinase deficiency anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
2913298015 | Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2913628019 | Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
3780591018 | Hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
4673191012 | PK (pyruvate kinase) deficiency hemolytic anemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
4673192017 | PK (pyruvate kinase) deficiency haemolytic anaemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
4673715012 | HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
4673717016 | HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Has interpretation | Present | true | Inferred relationship | Some | 3 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Interprets | Haemolysis | true | Inferred relationship | Some | 3 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Hereditary nonspherocytic haemolytic anaemia | true | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Deficiency of pyruvate kinase | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Associated etiologic finding | Enzymopathy | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Associated etiologic finding | Deficiency of pyruvate kinase | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Due to | Deficiency of pyruvate kinase | true | Inferred relationship | Some | 5 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Hereditary disorder of haematologic system | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Congenital anomaly of the haematopoietic system | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Inborn error of metabolism | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Is a | Anaemia due to enzyme deficiency | true | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Has definitional manifestation | Haemolysis | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Has interpretation | Below reference range | true | Inferred relationship | Some | 1 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Interprets | Red blood cell count | true | Inferred relationship | Some | 1 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Occurrence | Congenital | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Finding site | Erythrocyte | true | Inferred relationship | Some | 4 | |
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency | Interprets | Erythrocyte destruction | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set