Monoamine oxidase-A deficiency

Preferred Label : Monoamine oxidase-A deficiency;

ICD-11 definition : Monoamine oxidase-A deficiency is a very rare recessive X-linked biogenic amine metabolism disorder characterized clinically by mild intellectual deficit, impulsive aggressiveness, and sometimes violent behavior and presenting from childhood.;

Details

Origin ID

1742370445;

UMLS CUI

C0796275;

CISMeF manual mappings
- Monoamine oxidase A deficiency [ORDO Disease]
Currated CISMeF NLP mapping
- Brunner Syndrome [DO Concept]
- Brunner syndrome [OMIM Phenotype]
- Deficiency of monoamine oxidase A (disorder) [SNOMED CT concept]
- brunner syndrome [MeSH concept]
- brunner syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brunner Syndrome [DO Concept]
- Brunner syndrome [OMIM Phenotype]
- Brunner syndrome [MedDRA Preferred Term]
- Deficiency of monoamine oxidase A (disorder) [SNOMED CT concept]
- Monoamine oxidase A deficiency [ORDO Disease]
- brunner syndrome [MeSH concept]
- brunner syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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