OBO ID: DOID:0060573 |
Term Name: | von Willebrand's disease 1 | Search Ontology: | |
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Definition: | A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13. (2) | ||
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Ontology: | Human Disease (DOID:0060573) |
OTHER von Willebrand's disease 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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