190749000: Glucose-galactose malabsorption (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Glucose-galactose malabsorption
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Glucose-galactose malabsorption
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Glucose-galactose malabsorption
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption

\Finding of neonate\Neonatal disorder\...

\Neonatal metabolic disorder (disorder)\Glucose-galactose malabsorption

\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Glucose-galactose malabsorption
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Glucose-galactose malabsorption
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Glucose-galactose malabsorption
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Glucose-galactose malabsorption
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption
\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Neonatal metabolic disorder (disorder)\Glucose-galactose malabsorption
\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Glucose-galactose malabsorption
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Glucose-galactose malabsorption
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Glucose-galactose malabsorption
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Glucose-galactose malabsorption
\Disease\Metabolic disease\Neonatal metabolic disorder (disorder)\Glucose-galactose malabsorption
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Disorder of carbohydrate absorption\Malabsorption of glucose\Glucose-galactose malabsorption
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Disorder of carbohydrate transport\Malabsorption of glucose\Glucose-galactose malabsorption

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

Descriptions:

Id Description Lang Type Status Case? Module

293202016 Glucose-galactose malabsorption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

574369016 Glucose-galactose malabsorption (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5389616016 SGLT1 deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glucose-galactose malabsorption	Is a	Disorder of carbohydrate absorption	false	Inferred relationship	Some
Glucose-galactose malabsorption	Finding site	Body system structure	false	Inferred relationship	Some
Glucose-galactose malabsorption	Is a	Malabsorption of glucose	true	Inferred relationship	Some
Glucose-galactose malabsorption	Is a	Digestive system hereditary disorder (disorder)	true	Inferred relationship	Some
Glucose-galactose malabsorption	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Glucose-galactose malabsorption	Is a	Inborn error of metabolism	true	Inferred relationship	Some
Glucose-galactose malabsorption	Occurrence	Congenital	true	Inferred relationship	Some	3
Glucose-galactose malabsorption	Is a	Malabsorption syndrome	true	Inferred relationship	Some
Glucose-galactose malabsorption	Finding site	Gastrointestinal tract structure	true	Inferred relationship	Some	1
Glucose-galactose malabsorption	Is a	Neonatal gastrointestinal disorder	true	Inferred relationship	Some
Glucose-galactose malabsorption	Is a	Neonatal metabolic disorder (disorder)	true	Inferred relationship	Some
Glucose-galactose malabsorption	Occurrence	Neonatal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Malabsorption of glucose	Is a	False	Glucose-galactose malabsorption	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
293202016	Glucose-galactose malabsorption	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
574369016	Glucose-galactose malabsorption (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5389616016	SGLT1 deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core