238031009: Arylsulfatase A deficiency (disorder)

SNOMED CT Concept\constatation clinique\Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\Disorder of lipid storage and metabolism\Sphingolipidosis\Metachromatic leucodystrophy (disorder)\Arylsulfatase A deficiency

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

356777011 Severe deficiency of arylsulfatase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356778018 Severe deficiency of arylsulphatase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356779014 Arylsulfatase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356780012 Cerebroside sulphatase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356781011 ARSA - Arylsulphatase A deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

356782016 ARSA - Arylsulfatase A deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

356783014 Cerebroside sulfatase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356784015 Arylsulphatase A deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626853018 Arylsulfatase A deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Arylsulfatase A deficiency	est un(e) (attribut)	Metachromatic leucodystrophy (disorder)	true	Inferred relationship	Some
Arylsulfatase A deficiency	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Arylsulfatase A deficiency	survenue (attribut)	congénital	false	Inferred relationship	Some
Arylsulfatase A deficiency	est un(e) (attribut)	Metachromatic leukodystrophy	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Metachromatic leukodystrophy, adult type	est un(e) (attribut)	False	Arylsulfatase A deficiency	Inferred relationship	Some
Metachromatic leucodystrophy, juvenile type	est un(e) (attribut)	False	Arylsulfatase A deficiency	Inferred relationship	Some
Metachromatic leucodystrophy, late infantile type	est un(e) (attribut)	False	Arylsulfatase A deficiency	Inferred relationship	Some

This concept is not in any reference sets