OBO ID: DOID:0111056 |
Term Name: | platelet-type bleeding disorder 3 | Search Ontology: | |
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Definition: | A blood platelet disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has_material_basis_in mutation in the GP1BA gene on chromosome 17p13.2. (2) | ||
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Ontology: | Human Disease ( DOID:0111056 ) |
OTHER platelet-type bleeding disorder 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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