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Disease Ontology Browser
alpha-2-plasmin inhibitor deficiency (DOID:0060601)
Alliance: disease page
Synonyms: antiplasmin defiency; plasmin inhibitor deficiency
Alt IDs: OMIM:262850, ICD10CM:D68.8, ORDO:79
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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory