237967002: Lysosomal alpha-1,4-glucosidase deficiency (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

356657012 AMD - Acid maltase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

356658019 alpha-Glucosidase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

356659010 Glycogen storage disease type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356660017 alpha-1,4-Glucosidase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

356661018 Lysosomal alpha-1,4-glucosidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356662013 Acid maltase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626778013 Lysosomal alpha-1,4-glucosidase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease type II	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Glycogen storage disease type II	survenue (attribut)	congénital	false	Inferred relationship	Some
Glycogen storage disease type II	localisation d'une constatation (attribut)	foie	false	Inferred relationship	Some
Glycogen storage disease type II	localisation d'une constatation (attribut)	structure de muscle squelettique	false	Inferred relationship	Some
Glycogen storage disease type II	est un(e) (attribut)	maladie de stockage du glycogène (trouble)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Lysosomal alpha-1,4-glucosidase deficiency - infantile onset	est un(e) (attribut)	False	Glycogen storage disease type II	Inferred relationship	Some
Lysosomal alpha-1,4-glucosidase deficiency - juvenile onset	est un(e) (attribut)	False	Glycogen storage disease type II	Inferred relationship	Some
Lysosomal alpha-1,4-glucosidase deficiency - adult onset	est un(e) (attribut)	False	Glycogen storage disease type II	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)