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)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Glucose-galactose malabsorption (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Glucose-galactose malabsorption (disorder)
\Digestive system finding (finding)\Disease 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 (disorder)\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\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Neonatal metabolic disorder (disorder)\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Neonatal gastrointestinal disorder\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Glucose-galactose malabsorption (disorder)
\Disease\Disorder of body system\Disease 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	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Is a	Malabsorption of glucose	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Glucose-galactose malabsorption (disorder)	Is a	Malabsorption syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Finding site	Gastrointestinal tract structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Glucose-galactose malabsorption (disorder)	Is a	Neonatal gastrointestinal disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Is a	Neonatal metabolic disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-galactose malabsorption (disorder)	Occurrence	Neonatal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Malabsorption of glucose	Is a	False	Glucose-galactose malabsorption (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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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
293202016	Glucose-galactose malabsorption	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
293202016	Glucose-galactose malabsorption	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
293203014	Congenital monosaccharide malabsorption	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
293204015	Galactose intolerance	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
293204015	Galactose intolerance	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	Only initial character 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
3341101001000119	Glukose-Galaktose-Malabsorption	de	Synonym (core metadata concept)	Active	Entire term case sensitive (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
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
365781000195118	malassorbimento di glucosio-galattosio	it	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