Status: current, Primitive. Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3010526019 | Homozygous methylenetetrahydrofolate reductase mutation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3011447010 | Homozygous methylenetetrahydrofolate reductase mutation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Homozygous methylenetetrahydrofolate reductase mutation | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Homozygous methylenetetrahydrofolate reductase mutation | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
| Homozygous methylenetetrahydrofolate reductase mutation | Finding site | Structure of endocrine system | false | Inferred relationship | Some | ||
| Homozygous methylenetetrahydrofolate reductase mutation | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Homozygous methylenetetrahydrofolate reductase mutation | Finding site | Structure of endocrine system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR