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

• SNOMED CT Concept\Clinical finding (finding)\...
• \Neurological lesion\Leucodystrophy\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\...
• \Leucodystrophy\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Hereditary degenerative disease of central nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited metabolic disorder of nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Degenerative disorder\Degenerative disease of the central nervous system\Leucodystrophy\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited metabolic disorder of nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Leucodystrophy\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited metabolic disorder of nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary degenerative disease of central nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Leucodystrophy\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Lysosomal storage disease (disorder)\Sphingolipidosis\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \Disease\Metabolic disease\Enzymopathy\Lysosomal storage disease (disorder)\Sphingolipidosis\Metachromatic leukodystrophy\Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator
• \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, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
437768015	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
437769011	Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2788914016	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
437768015	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
437768015	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
437769011	Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
437769011	Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
692594010	Metachromatic leucodystrophy due to deficiency of cerebroside sulfatase activator (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2772269013	Metachromatic leucodystrophy due to deficiency of cerebroside sulfatase activator	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2788914016	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2788914016	Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6394121000241117	leucodystrophie métachromatique par déficit en activateur cérébroside sulfatase	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6394121000241117	leucodystrophie métachromatique par déficit en activateur cérébroside sulfatase	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

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