234422006: Acute intermittent porphyria (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Acute intermittent porphyria
• \Metabolic disease\Chronic metabolic disorder\Acute intermittent porphyria
• \Metabolic disease\Disorder of porphyrin metabolism\Porphyria\Acute intermittent porphyria
• \Metabolic disease\Disorder of porphyrin metabolism\Porphobilinogen deaminase deficiency\Acute intermittent porphyria
• \Chronic disease\Chronic metabolic disorder\Acute intermittent porphyria

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351223014	Acute intermittent porphyria	en	Synonym	Active	Case insensitive	SNOMED CT core
351224015	AIP - Acute intermittent porphyria	en	Synonym	Active	Case sensitive	SNOMED CT core
351225019	Pyrroloporphyria	en	Synonym	Active	Case insensitive	SNOMED CT core
351226018	Acute porphyria	en	Synonym	Active	Case insensitive	SNOMED CT core
351227010	Intermittent acute porphyria	en	Synonym	Active	Case insensitive	SNOMED CT core
351228017	Swedish porphyria	en	Synonym	Active	Case sensitive	SNOMED CT core
351229013	Intermittent acute porphyria syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
622738015	Acute intermittent porphyria (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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