Autosomal recessive hereditary disorder	Disorder of the urea cycle metabolism	Inborn error of metabolism	Specific enzyme deficiency
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Argininosuccinate lyase deficiency (disorder)
	Argininosuccinate lyase deficiency
	Argininosuccinic aciduria ASAL deficiency ASL deficiency Deficiency of argininosuccinate lyase
	argininosuccinaatlyasedeficiëntie

Id	41013004
Status	Primitive

Occurrence

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E72.2
Rule	TRUE
Advice	ALWAYS E72.2
Correlation	SNOMED CT source code to target map code correlation not specified