Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 399255019 | Congenital methemoglobinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 399256018 | Congenital methaemoglobinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 660181015 | Congenital methemoglobinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Congenital methemoglobinaema with defective methemoglobin-reducing system | Is a | True | Congenital methemoglobinemia | Inferred relationship | Existential restriction modifier | |
| Congenital methemoglobinemia with abnormal methemoglobins | Is a | True | Congenital methemoglobinemia | Inferred relationship | Existential restriction modifier | |
| Hereditary methemoglobinemia, enzymatic type | Is a | False | Congenital methemoglobinemia | Inferred relationship | Existential restriction modifier | |
| Hereditary methemoglobinemia due to globin chain mutation | Is a | True | Congenital methemoglobinemia | Inferred relationship | Existential restriction modifier | |
| Autosomal recessive congenital methemoglobinemia | Is a | True | Congenital methemoglobinemia | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets