Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3010526019 | Homozygous methylenetetrahydrofolate reductase mutation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3011447010 | Homozygous methylenetetrahydrofolate reductase mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Homozygous methylenetetrahydrofolate reductase mutation | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
| Homozygous methylenetetrahydrofolate reductase mutation | Finding site | Structure of endocrine system | false | Inferred relationship | Existential restriction modifier | ||
| Homozygous methylenetetrahydrofolate reductase mutation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Homozygous methylenetetrahydrofolate reductase mutation | Finding site | Structure of endocrine system | true | Inferred relationship | Existential restriction modifier | 1 | |
| Homozygous methylenetetrahydrofolate reductase mutation | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR