| monoamineoxidase A-deficiëntie (aandoening) | | monoamineoxidase A-deficiëntie | | syndroom van Brunner
MAO-A-deficiëntie
| | 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. |
| | Id | 718210003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E70.8 | | Term | Overige gespecificeerde stofwisselingsstoornissen van aromatische aminozuren |
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| SNOMED CT to Orphanet simple map | 3057 |
| SNOMED CT to ICD-10 extended map | | Target | E70.8 | | Rule | TRUE | | Advice | ALWAYS E70.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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