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27943000: Congenital glucose-galactose malabsorption (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
46787015 Congenital glucose-galactose malabsorption en Synonym Active Entire term case insensitive SNOMED CT core module
46788013 Congenital glucose-galactose intolerance en Synonym Active Entire term case insensitive SNOMED CT core module
758568015 Congenital glucose-galactose malabsorption (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital glucose-galactose malabsorption Is a Disorder of carbohydrate transport true Inferred relationship Existential restriction modifier
Congenital glucose-galactose malabsorption Finding site Body system structure false Inferred relationship Existential restriction modifier
Congenital glucose-galactose malabsorption Is a Congenital disease false Inferred relationship Existential restriction modifier
Congenital glucose-galactose malabsorption Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital glucose-galactose malabsorption Is a Congenital monosaccharide malabsorption true Inferred relationship Existential restriction modifier
Congenital glucose-galactose malabsorption Finding site Gastrointestinal tract structure true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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