Status: retired, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 117132014 | HNSHA due to NADH-methemoglobin reductase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 1364741000168115 | Hereditary nonspherocytic haemolytic anaemia due to reduced nicotinamide adenine dinucleotide-methaemoglobin reductase deficiency | en | Synonym | Active | Case insensitive | SNOMED Clinical Terms Australian extension |
| 1364751000168118 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methaemoglobin reductase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
| 2612550019 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methemoglobin reductase deficiency (disorder) | en | Fully specified name | Inactive | Initial character case insensitive | SNOMED CT core |
| 2621048016 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methemoglobin reductase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2621049012 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methemoglobin reductase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2914782015 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide-methemoglobin reductase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2915246015 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide-methemoglobin reductase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 501589013 | HNSHA due to NADH-methaemoglobin reductase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 810582016 | HNSHA due to NADH-methemoglobin reductase deficiency (disorder) | en | Fully specified name | Inactive | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| HNSHA due to NADH-methaemoglobin reductase deficiency | Is a | Hereditary nonspherocytic haemolytic anaemia | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Associated etiologic finding | Enzymopathy | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Due to | Enzymopathy | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Is a | Anaemia due to enzyme deficiency | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Is a | Hereditary methaemoglobinaemia, enzymatic type | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Is a | Erythrocyte enzyme deficiency | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Is a | Congenital anaemia | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Has definitional manifestation | Haemolysis | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Has interpretation | Below reference range | false | Inferred relationship | Some | 1 | |
| HNSHA due to NADH-methaemoglobin reductase deficiency | Interprets | Red blood cell count | false | Inferred relationship | Some | 1 | |
| HNSHA due to NADH-methaemoglobin reductase deficiency | Has interpretation | Below reference range | false | Inferred relationship | Some | 2 | |
| HNSHA due to NADH-methaemoglobin reductase deficiency | Interprets | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 2 | |
| HNSHA due to NADH-methaemoglobin reductase deficiency | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| HNSHA due to NADH-methaemoglobin reductase deficiency | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian dialect reference set
Concept inactivation indicator reference set
Description inactivation indicator reference set
REPLACED BY association reference set