Brunner Syndrome
Information
- Disease name
- Brunner Syndrome
- Disease ID
- DOID:0060693
- Description
- "An 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 Xp11." [url:https\://www.ncbi.nlm.nih.gov/pubmed/8211186, url:https\://www.ncbi.nlm.nih.gov/pubmed/8503438]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:9252
- Cross Reference ID (Disease Ontology)
- ICD10CM:E70.8
- Cross Reference ID (Disease Ontology)
- MESH:C563156
- Cross Reference ID (Disease Ontology)
- MIM:300615
- Cross Reference ID (Disease Ontology)
- ORDO:3057
- Exact Synonym (Disease Ontology)
- monoamine oxidase A deficiency