Monoamine oxidase a

Preferred Label : Monoamine oxidase a;

Symbol : MAOA;

CISMeF acronym : MAOA;

Type : Gene;

Alternative titles and symbols : Amine oxidase (flavin-containing) a;

Ensembl ID : ENSG00000189221;

Prefixed ID : *309850;

Details

Origin ID

309850;

UMLS CUI

C1417001;

Automatic exact mappings (from CISMeF team)
- Amine Oxidase [Flavin-Containing] A [NCIt concept]
- Amine oxidase (flavin-containing) (substance) [SNOMED CT concept]
- MAOA Gene [NCIt concept]
- MAOA wt Allele [NCIt concept]
- Monoamine oxidase [LOINC component]
- amine oxidase (flavin-containing) [SNOMED Notion]
- monoamine oxidase [MeSH concept]
- monoamine oxidase [MeSH Descriptor]
- monoamine oxidase A [ORDO Gene]
- monoamine oxidase A [HGNC gene]
False automatic mappings
- Methaqualone [NCIt concept]
HGNC gene
- monoamine oxidase A [HGNC gene]
Phenotypes related
- Brunner syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MAOA Gene [NCIt concept]
- monoamine oxidase A [ORDO Gene]
- monoamine oxidase A [HGNC gene]

Keyword's position in hierarchy(ies) :

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