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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
3607151000052117 medfödd monosackarid-malabsorption sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital monosaccharide malabsorption Is a Disorder of carbohydrate absorption true Inferred relationship Some
Congenital monosaccharide malabsorption Is a Congenital disease (disorder) true Inferred relationship Some
Congenital monosaccharide malabsorption Occurrence Congenital true Inferred relationship Some 1
Congenital monosaccharide malabsorption Is a Malabsorption syndrome true Inferred relationship Some
Congenital monosaccharide malabsorption Finding site Gastrointestinal tract structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital glucose-galactose malabsorption Is a True Congenital monosaccharide malabsorption Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

GB English

US English

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