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ONTOLOGY REPORT - ANNOTATIONS


Term:Brunner syndrome
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Accession:DOID:0060693 term browser browse the term
Definition: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. (DO)
Synonyms:exact_synonym: BRNRS;   monoamine oxidase A deficiency
 narrow_synonym: ANTISOCIAL BEHAVIOR, SUSCEPTIBILITY TO
 primary_id: MESH:C563156
 alt_id: OMIM:300615;   RDO:0012534
 xref: ORDO:3057
For additional species annotation, visit the Alliance of Genome Resources.


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Brunner syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Maoa monoamine oxidase A JBrowse link X 6,554,698 6,620,722 RGD:7240710
RGD:8554872

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Path 1
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  disease 14759
    syndrome 4210
      Brunner syndrome 1
Path 2
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  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        central nervous system disease 6892
          brain disease 6396
            disease of mental health 4314
              developmental disorder of mental health 2584
                specific developmental disorder 1319
                  intellectual disability 1146
                    Brunner syndrome 1
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