FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term alpha-2-plasmin inhibitor deficiency ID (Ontology) DOID:0060601 (Human Disease)
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.
Also Known As "antiplasmin defiency" ; "plasmin inhibitor deficiency"
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 Genes
 alpha-2-plasmin inhibitor deficiency       1
 for disease ribbon | alpha-2-plasmin inhibitor deficiency       1
 model of | alpha-2-plasmin inhibitor deficiency       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
blood coagulation disease        |
 |__hemorrhagic disease__________|
                                 alpha-2-plasmin inhibitor deficiency  1 rec.
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Is a autosomal recessive disease
hemorrhagic disease
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Synonyms
  • "antiplasmin defiency" EXACT
    "plasmin inhibitor deficiency" EXACT
Secondary IDs
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ICD10CM:D68.8
MIM:262850
ORDO:79