Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3304054016 | Hyperinsulinism and hyperammonemia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304055015 | Hyperinsulinism and hyperammonemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304056019 | Hyperinsulinism and hyperammonaemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5285668015 | GLUD1 related hyperinsulinism and hyperammonaemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5285669011 | Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5285670012 | GLUD1 related hyperinsulinism and hyperammonemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5285671011 | Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonaemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401675013 | A rare diffuse form of congenital hyperinsulinism characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia), chronic hyperammonemia and recurrent episodes of hypoglycemia induced by fasting and protein rich meals. Epilepsy and cognitive deficit, which are unrelated to hypoglycemia but possibly related to the chronic hyperammonemia, may also occur. This disorder is usually responsive to diazoxide treatment. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401676014 | A rare diffuse form of congenital hyperinsulinism characterised by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycaemia), chronic hyperammonaemia and recurrent episodes of hypoglycaemia induced by fasting and protein rich meals. Epilepsy and cognitive deficit, which are unrelated to hypoglycaemia but possibly related to the chronic hyperammonaemia, may also occur. This disorder is usually responsive to diazoxide treatment. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Hyperammonemia | true | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Hyperinsulinism | true | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Finding site | Endocrine pancreatic structure | false | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Hyperinsulinism and hyperammonemia syndrome (disorder) | Finding site | Endocrine pancreatic structure | true | Inferred relationship | Some | 1 | |
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Congenital disease (disorder) | false | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
Hyperinsulinism and hyperammonemia syndrome (disorder) | Is a | Disorder of digestive system specific to fetus OR newborn | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)