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55731008: Arylsulfatase deficiency without metachromatic leukodystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
92673013 Arylsulfatase deficiency without MLD en Synonym Active Only initial character case insensitive SNOMED CT core module
497380011 Arylsulphatase deficiency without MLD en Synonym Active Only initial character case insensitive SNOMED CT core module
2915125015 Arylsulfatase deficiency without metachromatic leukodystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2915128018 Arylsulfatase deficiency without metachromatic leukodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Arylsulfatase deficiency without metachromatic leukodystrophy Is a Disorder of lysosomal enzyme true Inferred relationship Existential restriction modifier
Arylsulfatase deficiency without metachromatic leukodystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Arylsulfatase deficiency without metachromatic leukodystrophy Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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