Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
105268016 | Glycine dehydrogenase (decarboxylating) deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
105269012 | Nonketotic hyperglycinemia, type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
105270013 | Glycine decarboxylase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
105271012 | P-protein deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
499553012 | P protein deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
499554018 | Glycine dehydrogenase decarboxylating deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
499555017 | Nonketotic hyperglycinaemia, type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
499556016 | Non-ketotic hyperglycinemia P protein deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
499557013 | Non-ketotic hyperglycinemia type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
499558015 | Non-ketotic hyperglycinaemia type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
499559011 | Non-ketotic hyperglycinaemia P protein deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
802600017 | Glycine dehydrogenase (decarboxylating) deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Glycine dehydrogenase (decarboxylating) deficiency | Is a | Enzymopathy | true | Inferred relationship | Some | ||
Glycine dehydrogenase (decarboxylating) deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Glycine dehydrogenase (decarboxylating) deficiency | Is a | Non-ketotic hyperglycinaemia | true | Inferred relationship | Some | ||
Glycine dehydrogenase (decarboxylating) deficiency | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
Glycine dehydrogenase (decarboxylating) deficiency | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Glycine dehydrogenase (decarboxylating) deficiency | Finding site | Body system structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set