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congenital plasminogen activator inhibitor type 1 deficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0013227

Congenital plasminogen activator inhibitor type 1 (PAI-1) deficiency is a rare genetic bleeding disorder characterized by premature lysis of hemostatic clots and a moderate bleeding tendency. [ Orphanet:465 ]

Synonyms: congenital PAI-1 deficiency congenital plasminogen activator inhibitor type 1 deficiency

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:717407006 (MONDO:equivalentTo)
  • GARD:4381 (Orphanet:465)
  • Orphanet:465 (OMIM:613329)
  • MESH:C567640 (MONDO:equivalentTo)
  • NCIT:C133884 (MONDO:equivalentTo)
  • OMIM:613329 (Orphanet:465/e)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4069

exactMatch

http://www.orpha.net/ORDO/Orphanet_465

http://identifiers.org/mesh/C567640

http://purl.obolibrary.org/obo/NCIT_C133884

http://identifiers.org/snomedct/717407006

https://omim.org/entry/613329

has related synonym

hyperfibrinolysis due to Pai1 deficiency

plasminogen activator inhibitor type 1 deficiency

plasminogen activator INHIBITOR-1 deficiency

id

MONDO:0013227

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0013227