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