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1228875006: Glucagon receptor-related hyperglucagonemia (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
5063551019 Mahvash disease en Synonym Active Case sensitive SNOMED CT core
5063552014 Glucagon receptor-related hyperglucagonaemia en Synonym Active Case insensitive SNOMED CT core
5063553016 GCGR-related hyperglucagonemia en Synonym Active Case sensitive SNOMED CT core
5063554010 GCGR-related hyperglucagonaemia en Synonym Active Case sensitive SNOMED CT core
5063555011 Glucagon receptor-related hyperglucagonemia en Synonym Active Case insensitive SNOMED CT core
5063556012 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 Case sensitive SNOMED CT core
5063557015 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
GCGR-related hyperglucagonaemia Is a Developmental hereditary disorder true Inferred relationship Some
GCGR-related hyperglucagonaemia Is a Digestive system hereditary disorder true Inferred relationship Some
GCGR-related hyperglucagonaemia Is a Hereditary disorder of endocrine system true Inferred relationship Some
GCGR-related hyperglucagonaemia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
GCGR-related hyperglucagonaemia Is a Hyperplasia of islet alpha cells with glucagon excess true Inferred relationship Some
GCGR-related hyperglucagonaemia Occurrence Congenital true Inferred relationship Some 1
GCGR-related hyperglucagonaemia Finding site Structure of alpha cell of islet true Inferred relationship Some 1
GCGR-related hyperglucagonaemia Associated morphology Hyperplasia true Inferred relationship Some 1
GCGR-related hyperglucagonaemia Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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