124628005: Deficiency of histidine ammonia-lyase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Deficiency of histidine ammonia-lyase
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Deficiency of histidine ammonia-lyase
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Deficiency of histidine ammonia-lyase
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of histidine metabolism\Deficiency of histidine ammonia-lyase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of histidine ammonia-lyase
• \Congenital disease\Inborn error of metabolism\Deficiency of histidine ammonia-lyase

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
204812012	Deficiency of histidine a-deaminase	en	Synonym	Active	Case insensitive	SNOMED CT core
204813019	Deficiency of histidinase	en	Synonym	Active	Case insensitive	SNOMED CT core
204814013	Deficiency of histidase	en	Synonym	Active	Case insensitive	SNOMED CT core
204815014	Deficiency of histidine ammonia-lyase	en	Synonym	Active	Case insensitive	SNOMED CT core
728346012	Deficiency of histidine ammonia-lyase (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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