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\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of glycine metabolism\Hyperglycinaemia\Non-ketotic hyperglycinaemia\Infantile glycine encephalopathy
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidaemia\Hyperglycinaemia\Non-ketotic hyperglycinaemia\Infantile glycine encephalopathy
• \Metabolic disease\Disorder of acid-base balance\Acidaemia\Aminoacidaemia\Hyperglycinaemia\Non-ketotic hyperglycinaemia\Infantile glycine encephalopathy

Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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