Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356606013 | TCN2 - Transcobalamin II deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 356607016 | Transcobalamin II deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 626738018 | Transcobalamin II deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Transcobalamin II deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Transcobalamin II deficiency | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Transcobalamin II deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Transcobalamin II deficiency | Is a | Vitamin disease | true | Inferred relationship | Some | ||
| Transcobalamin II deficiency | Is a | Disorder of sulfur-bearing amino acid metabolism | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital megaloblastic anaemia due to transcobalamin II deficiency | Due to | True | Transcobalamin II deficiency | Inferred relationship | Some | 4 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR