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450849003: Congenital monosaccharide malabsorption (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2012. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2920590011 Congenital monosaccharide malabsorption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2920890015 Congenital monosaccharide malabsorption (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital monosaccharide malabsorption est un(e) (attribut) Disorder of carbohydrate absorption true Inferred relationship Some
Congenital monosaccharide malabsorption est un(e) (attribut) Congenital disease true Inferred relationship Some
Congenital monosaccharide malabsorption survenue (attribut) congénital true Inferred relationship Some 1
Congenital monosaccharide malabsorption est un(e) (attribut) syndrome de malabsorption true Inferred relationship Some
Congenital monosaccharide malabsorption localisation d'une constatation (attribut) structure du tractus gastro-intestinal true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
malabsorption congénitale du glucose-galactose est un(e) (attribut) True Congenital monosaccharide malabsorption Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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