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 acidemia and trihydroxycholestanoic acidemia
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia
• \Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356856017	Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
356857014	Trihydroxycholestanoyl-CoA oxidase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
356858016	Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
626903011	Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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