238073001: Isolated alkyldihydroxyacetone phosphate synthase 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 alkyldihydroxyacetone phosphate synthase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Isolated alkyldihydroxyacetone phosphate synthase deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Isolated alkyldihydroxyacetone phosphate synthase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356861015	Isolated alkyldihydroxyacetone phosphate synthase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
626905016	Isolated alkyldihydroxyacetone phosphate synthase deficiency (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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