238071004: Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia
• \Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356856017	Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia	en	Synonym	Active	Case insensitive	SNOMED CT core
356857014	Trihydroxycholestanoyl-CoA oxidase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
356858016	Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
626903011	Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia (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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