aangeboren aminozuurstofwisselingsstoornis	autosomaal recessieve hereditaire aandoening	glutaaracidurie	hereditaire stoornis van metabolisme van zenuwstelsel	stoornis van lysine- en hydroxylysinemetabolisme
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deficiëntie van glutaryl-co-enzym A-dehydrogenase (aandoening)
	deficiëntie van glutaryl-co-enzym A-dehydrogenase
	glutaryl-CoA-dehydrogenasedeficiëntie deficiëntie van glutaryl-CoA-dehydrogenase
	Glutaryl-CoA dehydrogenase deficiency
	Glutaric aciduria type 1 Glutaric acidemia type 1 Glutaryl-coenzyme A dehydrogenase deficiency GCDH-gene related glutaryl-coenzyme A dehydrogenase deficiency GA I - glutaric aciduria type 1

Id	360416003
Status	Primitive

Occurrence

Finding site

structuur van systema nervosum

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E72.3
Term	Stoornissen van lysine- en hydroxylysinemetabolisme

SNOMED CT to Orphanet simple map

25

SNOMED CT to ICD-10 extended map

Target	E72.3
Rule	TRUE
Advice	ALWAYS E72.3
Correlation	SNOMED CT source code to target map code correlation not specified