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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:Kininogen Deficiency, High Molecular Weight and Low Molecular Weight
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Accession:DOID:9007477 term browser browse the term
Synonyms:primary_id: MESH:C567116



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Kininogen Deficiency, High Molecular Weight and Low Molecular Weight term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Kng1 kininogen 1 IAGP DNA:mutation:cds:p.Ala163Thr (rat) RGD PMID:11208766 RGD:68697 NCBI chr11:77,812,757...77,835,555
Ensembl chr11:77,812,752...77,835,555
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21120
    disease of anatomical entity 18195
      hematopoietic system disease 3339
        blood protein disease 595
          Kininogen Deficiency, High Molecular Weight and Low Molecular Weight 2
Path 2
Term Annotations click to browse term
  disease 21120
    disease of anatomical entity 18195
      Hemic and Lymphatic Diseases 3849
        hematopoietic system disease 3339
          blood protein disease 595
            Kininogen Deficiency, High Molecular Weight and Low Molecular Weight 2
paths to the root