415764005: Tyrosinemia type III (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Tyrosinaemia type III
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\4-Hydroxyphenylpyruvate dioxygenase deficiency\Tyrosinaemia type III
• \Metabolic disease\Enzymopathy\4-Hydroxyphenylpyruvate dioxygenase deficiency\Tyrosinaemia type III

Status: current, Primitive. Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2530083018	Tyrosinemia type III (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2533519017	Tyrosinemia type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2533520011	Tyrosinaemia type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3035359011	Tyrosinemia type 3	en	Synonym	Active	Case insensitive	SNOMED CT core
3035481017	Tyrosinaemia type 3	en	Synonym	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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