Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3671994016 | Congenital methemoglobinemia due to NADH-cytochrome b5 reductase 3 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3671995015 | Congenital NADH-methaemoglobin reductase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3672000015 | Congenital NADH-methemoglobin reductase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3672001016 | Cytochrome b5 reductase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3672016018 | Congenital methaemoglobinaemia due to NADH-cytochrome b5 reductase 3 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3672017010 | NADH-methaemoglobin reductase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3672018017 | NADH-methemoglobin reductase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3672019013 | Chronic familial methemoglobin reductase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3672020019 | Chronic familial methaemoglobin reductase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3672024011 | Autosomal recessive congenital methemoglobinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3672025012 | Autosomal recessive congenital methemoglobinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3672026013 | Autosomal recessive congenital methaemoglobinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive congenital methemoglobinemia | Is a | Hereditary red blood cell disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive congenital methemoglobinemia | Finding site | Erythrocyte | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive congenital methemoglobinemia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive congenital methemoglobinemia | Is a | Congenital methemoglobinemia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive congenital methemoglobinemia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal recessive congenital methemoglobinemia type II | Is a | True | Autosomal recessive congenital methemoglobinemia | Inferred relationship | Existential restriction modifier | |
| Autosomal recessive congenital methemoglobinemia type I | Is a | True | Autosomal recessive congenital methemoglobinemia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR