55731008: Arylsulfatase deficiency without metachromatic leukodystrophy (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of foetus and/or newborn\Congenital disease\Disorder of lysosomal enzyme\Arylsulphatase deficiency without metachromatic leucodystrophy

\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Arylsulphatase deficiency without metachromatic leucodystrophy

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

2915125015 Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2915128018 Arylsulfatase deficiency without metachromatic leukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5245570018 Arylsulfatase deficiency without MLD (metachromatic leukodystrophy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5245571019 Arylsulphatase deficiency without MLD (metachromatic leukodystrophy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5245720018 Arylsulphatase deficiency without metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

92673013 Arylsulfatase deficiency without MLD en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

497380011 Arylsulphatase deficiency without MLD en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

794146018 Arylsulfatase deficiency without MLD (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2915125015 Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2915125015 Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2915128018 Arylsulfatase deficiency without metachromatic leukodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2915128018 Arylsulfatase deficiency without metachromatic leukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5245570018 Arylsulfatase deficiency without MLD (metachromatic leukodystrophy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5245571019 Arylsulphatase deficiency without MLD (metachromatic leukodystrophy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5245720018 Arylsulphatase deficiency without metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5777881000241114 déficit en arylsulfatase sans leucodystrophie métachromatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5777881000241114 déficit en arylsulfatase sans leucodystrophie métachromatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Arylsulphatase deficiency without metachromatic leucodystrophy	Is a	Disorder of lysosomal enzyme	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Arylsulphatase deficiency without metachromatic leucodystrophy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Arylsulphatase deficiency without metachromatic leucodystrophy	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

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Active

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Characteristic

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Group

This concept is not in any reference sets