plasminogen activator Inhibitor-1 deficiency

Preferred Label : plasminogen activator Inhibitor-1 deficiency;

MeSH synonym : hyperfibrinolysis due to Pai1 deficiency;

Origin ID

C567640;

UMLS CUI

C2750067;

Automatic exact mappings (from CISMeF team)
- Plasminogen Activator Inhibitor-1 Deficiency [NCIt concept]
Currated CISMeF NLP mapping
- Congenital plasminogen activator inhibitor deficiency type 1 (disorder) [SNOMED CT concept]
- Congenital plasminogen activator inhibitor type 1 deficiency [ORDO Disease]
- Plasminogen activator inhibitor-1 deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- hemorrhagic disorders [MeSH Descriptor]
- plasminogen activator inhibitor 1 [MeSH Descriptor]
Record concept(s)
- plasminogen activator Inhibitor-1 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital plasminogen activator inhibitor type 1 deficiency [ORDO Disease]
- Plasminogen Activator Inhibitor-1 Deficiency [NCIt concept]
- Plasminogen activator inhibitor-1 deficiency [OMIM Phenotype]