Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3316394019 | Deficiency of dimethylglycine dehydrogenase (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3316395018 | Deficiency of dimethylglycine dehydrogenase | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3316396017 | Dimethylglycine dehydrogenase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5927431000146119 | dimethylglycinedehydrogenasedeficiëntie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 5927451000146113 | deficiëntie van dimethylglycinedehydrogenase | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8713451000146113 | deficiëntie van dimethylglycinedehydrogenase (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3316397014 | An extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3316398016 | An extremely rare autosomal recessive glycine metabolism disorder characterised clinically in the single reported case to date by muscle fatigue and a fish-like odour. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deficiency of dimethylglycine dehydrogenase (disorder) | Is a | Disorder of glycine metabolism | true | Inferred relationship | Some | ||
| Deficiency of dimethylglycine dehydrogenase (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Deficiency of dimethylglycine dehydrogenase (disorder) | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
| Deficiency of dimethylglycine dehydrogenase (disorder) | Is a | Hereditary metabolic disease | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR