55731008: Arylsulfatase deficiency without metachromatic leukodystrophy (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Arylsulfatase deficiency without metachromatic leukodystrophy
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Arylsulfatase deficiency without metachromatic leukodystrophy
• \Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Arylsulfatase deficiency without metachromatic leukodystrophy
• \Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Arylsulfatase deficiency without metachromatic leukodystrophy

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1983371000168115	Arylsulfatase deficiency without metachromatic leucodystrophy	en	Synonym	Active	Case insensitive	SNOMED Clinical Terms Australian extension
2915125015	Arylsulfatase deficiency without metachromatic leukodystrophy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2915128018	Arylsulfatase deficiency without metachromatic leukodystrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
497380011	Arylsulphatase deficiency without MLD	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
92673013	Arylsulfatase deficiency without MLD	en	Synonym	Active	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

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