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39998009: Verner-Morrison syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


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 Existential restriction modifier
Verner-Morrison syndrome Finding site Endocrine pancreatic structure true Inferred relationship Existential restriction modifier 1
Verner-Morrison syndrome Finding site Structure of digestive system false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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