Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 399255019 | Congenital methemoglobinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 399256018 | Congenital methaemoglobinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 660181015 | Congenital methemoglobinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital methaemoglobinaemia | Finding site | Erythrocyte | true | Inferred relationship | Some | 2 | |
| Congenital methaemoglobinaemia | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Congenital methaemoglobinaemia | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Congenital methaemoglobinaemia | Is a | Congenital anomaly of the haematopoietic system | false | Inferred relationship | Some | ||
| Congenital methaemoglobinaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital methaemoglobinaemia | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital methaemoglobinaemia | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
| Congenital methaemoglobinaemia | Is a | Methaemoglobinaemia | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary methaemoglobinaemia, enzymatic type | Is a | False | Congenital methaemoglobinaemia | Inferred relationship | Some | |
| Congenital methaemoglobinaema with defective methaemoglobin-reducing system | Is a | True | Congenital methaemoglobinaemia | Inferred relationship | Some | |
| Congenital methaemoglobinaemia with abnormal methaemoglobins | Is a | True | Congenital methaemoglobinaemia | Inferred relationship | Some | |
| Haemoglobin M disease | Is a | True | Congenital methaemoglobinaemia | Inferred relationship | Some | |
| Autosomal recessive congenital methaemoglobinaemia | Is a | True | Congenital methaemoglobinaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR