OBO ID: DOID:12531 |
Term Name: | von Willebrand's disease | Search Ontology: | |
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Definition: | A blood coagulation disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. (2) | ||
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Ontology: | Human Disease ( DOID:12531 ) |
OTHER von Willebrand's disease PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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vwfunt2/+ | light ablation: blood | Iyer et al., 2019 |
physical alteration: caudal vein | Iyer et al., 2019 |
PHENOTYPE
No data available
CITATIONS (1)
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