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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Plasminogen Activator Inhibitor-1 Deficiency
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Accession:DOID:9008533 term browser browse the term
Synonyms:exact_synonym: Hyperfibrinolysis Due To Pai1 Deficiency
 primary_id: MESH:C567640;   RDO:0015656
 alt_id: OMIM:613329
 xref: NCI:C133884
For additional species annotation, visit the Alliance of Genome Resources.


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Plasminogen Activator Inhibitor-1 Deficiency term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ap1s1 adaptor related protein complex 1 subunit sigma 1 ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY ClinVar PMID:21681106 NCBI chrNW_004955456:16,127,877...16,134,039
Ensembl chrNW_004955456:16,127,877...16,134,039
JBrowse link
G Mogat3 monoacylglycerol O-acyltransferase 3 ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY ClinVar PMID:21681106 NCBI chrNW_004955456:16,090,859...16,094,736 JBrowse link
G Nat16 N-acetyltransferase 16 (putative) ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY ClinVar PMID:21681106 NCBI chrNW_004955456:16,114,681...16,118,249 JBrowse link
G Plod3 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY ClinVar PMID:21681106 NCBI chrNW_004955456:16,082,424...16,090,773
Ensembl chrNW_004955456:16,082,437...16,093,389
JBrowse link
G Serpine1 serpin family E member 1 ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY OMIM
ClinVar
PMID:1435917 PMID:9207454 PMID:12856128 PMID:15650551 PMID:17656673 More... NCBI chrNW_004955456:16,147,523...16,157,040
Ensembl chrNW_004955456:16,145,944...16,157,142
JBrowse link
G Trim56 tripartite motif containing 56 ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY ClinVar PMID:21681106 NCBI chrNW_004955456:16,181,890...16,185,598
Ensembl chrNW_004955456:16,182,453...16,184,669
JBrowse link
G Vgf VGF nerve growth factor inducible ISO ClinVar Annotator: match by term: HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY ClinVar PMID:21681106 NCBI chrNW_004955456:16,119,073...16,126,968
Ensembl chrNW_004955456:16,119,073...16,126,968
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13345
    disease of anatomical entity 13084
      hematopoietic system disease 2356
        blood coagulation disease 723
          hemorrhagic disease 694
            Plasminogen Activator Inhibitor-1 Deficiency 7
Path 2
Term Annotations click to browse term
  disease 13345
    disease of anatomical entity 13084
      Hemic and Lymphatic Diseases 2737
        hematopoietic system disease 2356
          blood coagulation disease 723
            hemorrhagic disease 694
              Plasminogen Activator Inhibitor-1 Deficiency 7
paths to the root