Search Ontology:
Human Disease

alpha-2-plasmin inhibitor deficiency

Term ID
DOID:0060601
Synonyms
  • antiplasmin defiency
  • plasmin inhibitor deficiency
Definition
A hemorrhagic disease that has_material_basis_in mutation in the PLI gene. It is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes. (2)
References
Ontology
Human Disease   ( DOID:0060601 )
Relationships
is a type of
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Genes Involved
Zebrafish Models