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39998009: Verner-Morrison syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3433664019 Pancreatic cholera en Synonym Active Case insensitive SNOMED CT core
492365011 Werner Morrison syndrome en Synonym Active Case sensitive SNOMED CT core
492366012 Excessive vasoactive intestinal peptide secretion en Synonym Active Case insensitive SNOMED CT core
66617010 Verner-Morrison syndrome en Synonym Active Case sensitive SNOMED CT core
66618017 WDHA syndrome en Synonym Active Case sensitive SNOMED CT core
776557012 Verner-Morrison syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Verner-Morrison syndrome Is a Disorder of endocrine pancreas true Inferred relationship Some
Verner-Morrison syndrome Finding site Structure of digestive system false Inferred relationship Some
Verner-Morrison syndrome Finding site Endocrine pancreatic structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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