271847005: Hereditary hypertyrosinemia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary hypertyrosinaemia
• \Metabolic disease\Hereditary metabolic disease\Hereditary hypertyrosinaemia
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidaemia\Hypertyrosinaemia\Hereditary hypertyrosinaemia
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\Hypertyrosinaemia\Hereditary hypertyrosinaemia
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Aminoacidaemia\Hypertyrosinaemia\Hereditary hypertyrosinaemia

Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
406832013	Tyrosinaemia-tyrosiluria hereditary syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
406833015	Hereditary hypertyrosinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
406834014	Hereditary hypertyrosinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
406835010	Tyrosinemia-tyrosiluria hereditary syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
4554512018	Hereditary tyrosinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
4554513011	Hereditary tyrosinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
664301017	Hereditary hypertyrosinemia (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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