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ONTOLOGY REPORT - ANNOTATIONS


Term:von Willebrand's disease
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Accession:DOID:12531 term browser browse the term
Definition:Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Synonyms:exact_synonym: Angiohemophilia;   Angiohemophilias;   Vascular Hemophilia;   Vascular Hemophilias;   Vascular Pseudohemophilia;   Vascular Pseudohemophilias;   Von Willebrand Disorder;   Von Willebrand's Factor Deficiency;   von Willebrand Disease;   von Willebrand Disease, Recessive Form;   von Willebrand diseases;   von Willebrand's Diseases;   von Willebrand's-Jurgens' disease;   von Willebrand-Jrgens disease
 primary_id: MESH:D014842;   RDO:0000238
 xref: GARD:7867;   NCI:C68677
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von Willebrand's disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G F3 coagulation factor III, tissue factor JBrowse link 2 225,310,686 225,322,281 RGD:11341671
G Vwf von Willebrand factor JBrowse link 4 158,085,059 158,219,525 RGD:1331525
RGD:11079196
RGD:8554872
platelet-type bleeding disorder 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gp1ba glycoprotein Ib platelet subunit alpha JBrowse link 10 57,260,680 57,263,546 RGD:7240710
RGD:10450823
RGD:10450814
RGD:10450803
RGD:8554872
von Willebrand's disease 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Itga2 integrin subunit alpha 2 JBrowse link 2 46,996,904 47,097,011 RGD:10766468
RGD:11530070
G Itga2b integrin subunit alpha 2b JBrowse link 10 90,397,960 90,416,550 RGD:10766468
G Plat plasminogen activator, tissue type JBrowse link 16 74,098,263 74,122,897 RGD:11552591
G Vwf von Willebrand factor JBrowse link 4 158,085,059 158,219,525 RGD:7240710
RGD:8554872
RGD:10766468
RGD:11079205
von Willebrand's disease 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G F8 coagulation factor VIII JBrowse link 18 367,862 399,242 RGD:10766469
G Itga2 integrin subunit alpha 2 JBrowse link 2 46,996,904 47,097,011 RGD:10766469
G Itga2b integrin subunit alpha 2b JBrowse link 10 90,397,960 90,416,550 RGD:10766469
G Vwf von Willebrand factor JBrowse link 4 158,085,059 158,219,525 RGD:7240710
RGD:8554872
RGD:10766469
RGD:11079206
RGD:11079203
RGD:11079202
RGD:11079201
RGD:11079200
von Willebrand's disease 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Vwf von Willebrand factor JBrowse link 4 158,085,059 158,219,525 RGD:7240710
RGD:8554872
RGD:11079204

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      hematopoietic system disease 1426
        hemorrhagic disease 430
          von Willebrand's disease 7
            Von Willebrand Disease, X-Linked Form 0
            Von Willebrand Factor, Deficiency 0
            platelet-type bleeding disorder 3 1
            von Willebrand's disease 1 4
            von Willebrand's disease 2 4
            von Willebrand's disease 3 1
Path 2
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      Hemic and Lymphatic Diseases 1704
        hematopoietic system disease 1426
          blood coagulation disease 444
            hemorrhagic disease 430
              blood platelet disease 191
                von Willebrand's disease 7
                  Von Willebrand Disease, X-Linked Form 0
                  Von Willebrand Factor, Deficiency 0
                  platelet-type bleeding disorder 3 1
                  von Willebrand's disease 1 4
                  von Willebrand's disease 2 4
                  von Willebrand's disease 3 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.