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722302009: Glycogen storage disease type II infantile onset (disorder)


Status: current, 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
3331990013 Glycogen storage disease due to acid maltase deficiency, infantile onset en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331991012 Glycogenosis due to acid maltase deficiency, infantile onset en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331992017 Glycogenosis type II, infantile onset en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331993010 Pompe disease, infantile onset en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331994016 Glycogen storage disease type II infantile onset (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334442014 Glycogen storage disease type II infantile onset en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331988012 Glycogen storage disease (GSD) due to acid maltase deficiency, classical infantile onset (AMDI), is the most severe form of glycogen storage disease due to acid maltase deficiency. Characterized by cardiomegaly with respiratory distress, muscle weakness and feeding difficulties, it is potentially fatal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3332474015 Glycogen storage disease (GSD) due to acid maltase deficiency, classical infantile onset (AMDI), is the most severe form of glycogen storage disease due to acid maltase deficiency. Characterised by cardiomegaly with respiratory distress, muscle weakness and feeding difficulties, it is potentially fatal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glycogen storage disease due to acid maltase deficiency, infantile onset est un(e) (attribut) Glycogen storage disease due to acid maltase deficiency true Inferred relationship Some
Glycogen storage disease due to acid maltase deficiency, infantile onset survenue (attribut) congénital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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