# Brunner Syndrome

> amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has material basis in mutation in the MAOA gene on chromosome location Xp11

**Wikidata**: [Q4979092](https://www.wikidata.org/wiki/Q4979092)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Brunner_syndrome)  
**Source**: https://4ort.xyz/entity/brunner-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/20ffc014-ef31-4693-91c4-424bbe1e48dd--2020-04-14T20:39:50)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_20ffc014-ef31-4693-91c4-424bbe1e48dd-2020-04-14T203950.820Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000189221/MONDO_0010379)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000189221/Orphanet_3057)
9. [Identifiers.org](https://registry.identifiers.org/registry/doid)