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 |
| 399255019 | Congenital methemoglobinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 399256018 | Congenital methaemoglobinaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 660181015 | Congenital methemoglobinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1298451000052115 | kongenital methemoglobinemi | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital methemoglobinemia | Is a | Methemoglobinemia | true | Inferred relationship | Some | ||
| Congenital methemoglobinemia | Finding site | Erythrocyte | true | Inferred relationship | Some | 2 | |
| Congenital methemoglobinemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Congenital methemoglobinemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Congenital methemoglobinemia | Is a | Congenital anomaly of the hematopoietic system | false | Inferred relationship | Some | ||
| Congenital methemoglobinemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital methemoglobinemia | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Congenital methemoglobinemia | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital methaemoglobinaema with defective methaemoglobin-reducing system | Is a | True | Congenital methemoglobinemia | Inferred relationship | Some | |
| Congenital methemoglobinemia with abnormal methemoglobins | Is a | True | Congenital methemoglobinemia | Inferred relationship | Some | |
| ärftlig methemoglobinemi, enzymatisk typ | Is a | False | Congenital methemoglobinemia | Inferred relationship | Some | |
| Hemoglobin M disease | Is a | True | Congenital methemoglobinemia | Inferred relationship | Some | |
| Autosomal recessive congenital methemoglobinemia (disorder) | Is a | True | Congenital methemoglobinemia | Inferred relationship | Some |
This concept is not in any reference sets
FHIR