Plasminogen Activator Inhibitor-1 Deficiency

Preferred Label : Plasminogen Activator Inhibitor-1 Deficiency;

NCIt definition : An autosomal recessive condition caused by mutation(s) in the PAI1 gene, encoding plasminogen activator inhibitor 1. It is characterized by increased bleeding following trauma, injury, or surgery and in women, menorrhagia.;

Details

Origin ID

C133884;

UMLS CUI

C2750067;

Automatic exact mappings (from CISMeF team)
- Plasminogen activator inhibitor-1 deficiency [OMIM Phenotype]
- plasminogen activator Inhibitor-1 deficiency [MeSH concept]
- plasminogen activator Inhibitor-1 deficiency [MeSH Supplementary Concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt 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 [OMIM Phenotype]
- plasminogen activator Inhibitor-1 deficiency [MeSH Supplementary Concept]
- plasminogen activator Inhibitor-1 deficiency [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]
disease_mapped_to_gene
- SERPINE1 Gene [NCIt concept]

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