28183005: Fructose-biphosphatase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Fructose-1,6-bisphosphatase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fructose-1,6-bisphosphatase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Fructose-1,6-bisphosphatase deficiency
• \Metabolic disease\Enzymopathy\Fructose-1,6-bisphosphatase deficiency
• \Metabolic disease\Disorder of carbohydrate metabolism\Fructose metabolism disorder\Fructose-1,6-bisphosphatase deficiency
• \Congenital disease\Inborn error of metabolism\Fructose-1,6-bisphosphatase deficiency

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1225814015	Fructose-1,6-bisphosphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
4192201000168116	FBP - Fructose-1,6-bisphosphatase deficiency	en	Synonym	Active	Case sensitive	SNOMED Clinical Terms Australian extension
4192211000168118	HFBP - Hereditary fructose-1,6-bisphosphatase deficiency	en	Synonym	Active	Case sensitive	SNOMED Clinical Terms Australian extension
47181017	Fructose-biphosphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
47182012	Fructose-1,6-diphosphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
47183019	Hereditary fructose-1,6-phosphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
758834017	Fructose-biphosphatase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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