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722343009: Glycogen storage disease type II late onset (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3331996019 Glycogen storage disease type II late onset (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3331997011 Glycogen storage disease type II late onset en Synonym Active Only initial character case insensitive SNOMED CT core module
3331998018 Glycogen storage disease due to acid maltase deficiency, late-onset en Synonym Active Entire term case insensitive SNOMED CT core module
3331999014 Alpha-1,4-glucosidase acid deficiency, late onset en Synonym Active Entire term case insensitive SNOMED CT core module
3332000015 Glycogenosis type II, late onset en Synonym Active Only initial character case insensitive SNOMED CT core module
3332001016 Pompe disease, late onset en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease type II late onset Is a Glycogen storage disease, type II true Inferred relationship Existential restriction modifier
Glycogen storage disease type II late onset Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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