1156826003: Infantile glycine encephalopathy (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Infantile glycine encephalopathy
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of glycine metabolism\Hyperglycinemia\Non-ketotic hyperglycinemia\Infantile glycine encephalopathy
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidemia\Hyperglycinemia\Non-ketotic hyperglycinemia\Infantile glycine encephalopathy
• \Metabolic disease\Disorder of acid-base balance\Acidemia\Aminoacidemia\Hyperglycinemia\Non-ketotic hyperglycinemia\Infantile glycine encephalopathy

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4576275010	Infantile glycine encephalopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4576277019	Infantile glycine encephalopathy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4579183014	Infantile non-ketotic hyperglycinaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4579184015	Infantile non-ketotic hyperglycinemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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