238072006: Isolated dihydroxyacetone phosphate acyltransferase deficiency (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\Isolated dihydroxyacetone phosphate acyltransferase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Isolated dihydroxyacetone phosphate acyltransferase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Isolated dihydroxyacetone phosphate acyltransferase deficiency

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
356859012	Isolated DHAP-AT - dihydroxyacetone phosphate acyltransferase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
356860019	Isolated dihydroxyacetone phosphate acyltransferase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
626904017	Isolated dihydroxyacetone phosphate acyltransferase deficiency (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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