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47683004: Metachromatic leukodystrophy, late infantile type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1230504012 Late infantile metachromatic leucodystrophy en Synonym Active Case insensitive SNOMED CT core
1788033010 Greenfield disease en Synonym Active Case sensitive SNOMED CT core
494894011 Metachromatic leucodystrophy, late infantile type en Synonym Active Case insensitive SNOMED CT core
785168018 Metachromatic leukodystrophy, late infantile type (disorder) en Fully specified name Active Case insensitive SNOMED CT core
79462015 Metachromatic leukodystrophy, late infantile type en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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