410056006: Tyrosinemia type I (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Hereditary hypertyrosinaemia\Tyrosinaemia type I
• \Hereditary neoplastic syndrome\Tyrosinaemia type I
• \Metabolic disease\Hereditary metabolic disease\Hereditary hypertyrosinaemia\Tyrosinaemia type I
• \Metabolic disease\Clinical manifestation of enzyme deficiency\Tyrosinaemia type I
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidaemia\Hypertyrosinaemia\Hereditary hypertyrosinaemia\Tyrosinaemia type I
• \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\Tyrosinaemia type I
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Aminoacidaemia\Hypertyrosinaemia\Hereditary hypertyrosinaemia\Tyrosinaemia type I

Status: current, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2465507011	Tyrosinemia type I (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2469188016	Tyrosinaemia type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2469662018	Tyrosinemia type I	en	Synonym	Active	Initial character 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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