brunner syndrome

Preferred Label : brunner syndrome;

MeSH note : mutation in monoamine oxidase A (MAOA);

Origin ID

C563156;

UMLS CUI

C0796275;

Automatic exact mappings (from CISMeF team)
- Brown's tendon sheath syndrome (disorder) [SNOMED CT concept]
- Brunner syndrome [MedDRA Preferred Term]
- Bruns' syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Brunner Syndrome [DO Concept]
- Brunner syndrome [OMIM Phenotype]
- Deficiency of monoamine oxidase A (disorder) [SNOMED CT concept]
- Monoamine oxidase A deficiency [ORDO Disease]
- Monoamine oxidase-A deficiency [ICD-11 More detail]
DO Cross reference
- Brunner Syndrome [DO Concept]
MeSH term(s) associated for indexing
- Disruptive, Impulse Control, and Conduct Disorders [MeSH Descriptor]
- aggression [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- monoamine oxidase [MeSH Descriptor]
Record concept(s)
- brunner syndrome [MeSH 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]
- Monoamine oxidase-A deficiency [ICD-11 More detail]