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

\Finding of neonate\Neonatal disorder\...

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

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

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

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glucose-galactose malabsorption (disorder)	Is a	Disorder of carbohydrate absorption	false	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Finding site	Body system structure	false	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Is a	Malabsorption of glucose	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Is a	Digestive system hereditary disorder	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Is a	Inborn error of metabolism	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	3
Glucose-galactose malabsorption (disorder)	Is a	Malabsorption syndrome	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Finding site	Oesophagus, stomach, small intestine and large intestine together as a single entity.	true	Inferred relationship	Some	1
Glucose-galactose malabsorption (disorder)	Is a	Neonatal gastrointestinal disorder	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Is a	Neonatal metabolic disorder (disorder)	true	Inferred relationship	Some
Glucose-galactose malabsorption (disorder)	Occurrence	Neonatal	true	Inferred relationship	Some	1

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

Reference Sets

Description inactivation indicator reference set

GB English

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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
365781000195118	malassorbimento di glucosio-galattosio	it	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3541000172110	malabsorption du glucose-galactose	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
50004411000188114	intolérance au galactose	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3341101001000119	Glukose-Galaktose-Malabsorption	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module