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About: Brunner Syndrome     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • Brunner Syndrome
described by
id
  • DOID:0060693
database_cross_reference
  • ICD10CM:E70.8
  • MESH:C563156
  • OMIM:300615
  • ORDO:3057
has_exact_synonym
  • monoamine oxidase A deficiency (en)
has_obo_namespace
  • disease_ontology
in_subset
http://purl.obolib...g/obo/IAO_0000115
  • 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.
is topic of
is annotatedSource of
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