Category:Glutaric aciduria type 1

**glutaric aciduria type 1**
	Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder
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Instance of	designated intractable/rare disease; rare disease; class of disease;
Subclass of	cerebral organic aciduria; neurometabolic disease; Glutaric aciduria; organic acidemia; autosomal recessive disease;
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	Q2140501;
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Media in category "Glutaric aciduria type 1"

The following 2 files are in this category, out of 2 total.