Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5063550018 | Glucagon receptor-related hyperglucagonemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5063551019 | Mahvash disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5063552014 | Glucagon receptor-related hyperglucagonaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5063553016 | GCGR-related hyperglucagonemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5063554010 | GCGR-related hyperglucagonaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5063555011 | Glucagon receptor-related hyperglucagonemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400052011 | A rare tumor of pancreas caused by mutations in the GCGR gene characterized by pancreatic alpha cell hyperplasia, pancreatic neuroendocrine tumors and markedly increased serum glucagon levels in the absence of a glucagonoma syndrome. Clinical manifestations may include abdominal pain, pancreatitis, fatigue, diarrhea, and diabetes mellitus. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400053018 | A rare tumour of pancreas caused by mutations in the GCGR gene characterised by pancreatic alpha cell hyperplasia, pancreatic neuroendocrine tumours and markedly increased serum glucagon levels in the absence of a glucagonoma syndrome. Clinical manifestations may include abdominal pain, pancreatitis, fatigue, diarrhoea, and diabetes mellitus. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Glucagon receptor-related hyperglucagonemia (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Glucagon receptor-related hyperglucagonemia (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Glucagon receptor-related hyperglucagonemia (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Glucagon receptor-related hyperglucagonemia (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Glucagon receptor-related hyperglucagonemia (disorder) | Is a | Hyperplasia of islet alpha cells with glucagon excess | true | Inferred relationship | Some | ||
Glucagon receptor-related hyperglucagonemia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Glucagon receptor-related hyperglucagonemia (disorder) | Finding site | Structure of alpha cell of islet | true | Inferred relationship | Some | 1 | |
Glucagon receptor-related hyperglucagonemia (disorder) | Associated morphology | Hyperplasia | true | Inferred relationship | Some | 1 | |
Glucagon receptor-related hyperglucagonemia (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)