297278001: Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Sphingolipidosis\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1984481000168111	Metachromatic leucodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym	Active	Case insensitive	SNOMED Clinical Terms Australian extension
2772269013	Metachromatic leucodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2788914016	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
437768015	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym	Active	Case insensitive	SNOMED CT core
437769011	Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator	en	Synonym	Active	Case insensitive	SNOMED CT core
692594010	Metachromatic leucodystrophy due to deficiency of cerebroside sulfatase activator (disorder)	en	Fully specified name	Inactive	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start