Deficiency of tyraminase	Inherited metabolic disorder of nervous system	X-linked recessive hereditary disease
\|	\|	\|

Deficiency of monoamine oxidase A (disorder)
	Brunner syndrome
	Deficiency of monoamine oxidase A Monoamine oxidase A deficiency
	A very rare recessive X-linked biogenic amine metabolism disorder with clinical characteristics of mild intellectual deficit, impulsive aggressiveness, sometimes violent behavior and presenting from childhood.
	monoamineoxidase A-deficiëntie
	MAO-A-deficiëntie syndroom van Brunner

Id	718210003
Status	Primitive

Occurrence

Finding site

Structure of nervous system

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E70.8
Rule	TRUE
Advice	ALWAYS E70.8
Correlation	SNOMED CT source code to target map code correlation not specified