Search Ontology:
Human Disease

hereditary alpha tryptasemia syndrome

Term ID
DOID:0080714
Synonyms
Definition
A syndrome that is characterized by high blood tryptase levels and that has_material_basis_in inherited extra copies of the alpha tryptase gene (TPSAB1), effecting multiple organ systems including skin and connective tissues, the gastrointestinal and cardiovascular systems. (4)
References
  • GARD:13193
Ontology
Human Disease   ( DOID:0080714 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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