| Metadata | |
|---|---|
| ID | DOID:0060693 |
| Name | Brunner Syndrome |
| Definition | An amino acid metabolic disorder characterized by recessive X-linked inheritance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11. https://www.ncbi.nlm.nih.gov/pubmed/8503438, https://www.ncbi.nlm.nih.gov/pubmed/8211186 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
monoamine oxidase A deficiency [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some X-linked recessive inheritance |