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367641000119101: Increased gastrin secretion (disorder)


Status: current, Defined. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3013485015 Increased gastrin secretion en Synonym Active Case insensitive SNOMED CT core
3013492013 Increased gastrin secretion (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3013493015 Hypergastrinemia en Synonym Active Case insensitive SNOMED CT core
3951201010 Hypergastrinaemia en Synonym Active Case insensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypergastrinaemia Interprets Gastrin secretion, function true Inferred relationship Some 1
Hypergastrinaemia Has interpretation Abnormally high true Inferred relationship Some 1
Hypergastrinaemia Interprets Evaluation procedure false Inferred relationship Some 3
Hypergastrinaemia Is a Disorder of endocrine system true Inferred relationship Some
Hypergastrinaemia Finding site Entire G cell of digestive tract true Inferred relationship Some 2
Hypergastrinaemia Interprets Endocrine observable false Inferred relationship Some 3
Hypergastrinaemia Is a Increased hormone secretion false Inferred relationship Some
Hypergastrinaemia Is a Abnormality of secretion of gastrin true Inferred relationship Some
Hypergastrinaemia Finding site Endocrine pancreatic structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypergastrinaemia due to drug Is a True Hypergastrinaemia Inferred relationship Some
Familial hypergastrinaemic duodenal ulcer Is a True Hypergastrinaemia Inferred relationship Some
Zollinger-Ellison syndrome Is a True Hypergastrinaemia Inferred relationship Some
Hyperplasia of islet alpha cells with gastrin excess Is a True Hypergastrinaemia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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