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238031009: Arylsulfatase A deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
356777011 Severe deficiency of arylsulfatase en Synonym Active Case insensitive SNOMED CT core
356778018 Severe deficiency of arylsulphatase en Synonym Active Case insensitive SNOMED CT core
356779014 Arylsulfatase A deficiency en Synonym Active Initial character case insensitive SNOMED CT core
356780012 Cerebroside sulphatase deficiency en Synonym Active Case insensitive SNOMED CT core
356781011 ARSA - Arylsulphatase A deficiency en Synonym Active Case sensitive SNOMED CT core
356782016 ARSA - Arylsulfatase A deficiency en Synonym Active Case sensitive SNOMED CT core
356783014 Cerebroside sulfatase deficiency en Synonym Active Case insensitive SNOMED CT core
356784015 Arylsulphatase A deficiency en Synonym Active Initial character case insensitive SNOMED CT core
626853018 Arylsulfatase A deficiency (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Arylsulfatase A deficiency Is a Metachromatic leukodystrophy true Inferred relationship Some
Arylsulfatase A deficiency Finding site Body system structure false Inferred relationship Some
Arylsulfatase A deficiency Occurrence Congenital false Inferred relationship Some
Arylsulfatase A deficiency Is a Metachromatic leukodystrophy false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Metachromatic leucodystrophy, adult type Is a False Arylsulfatase A deficiency Inferred relationship Some
Metachromatic leucodystrophy, juvenile type Is a False Arylsulfatase A deficiency Inferred relationship Some
Metachromatic leucodystrophy, late infantile type Is a False Arylsulfatase A deficiency Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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