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General Information
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| Term |
platelet-type bleeding disorder 3 |
ID (Ontology) |
DOID:0111056 (Human Disease) |
| 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. |
| Also Known As |
"BDPLT3" ; "platelet type-von Willebrand disease" ; "pseudo-von Willebrand disease" (for all, see Synonyms field below) |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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platelet-type bleeding disorder 3 | 1 | for disease ribbon | platelet-type bleeding disorder 3 | 1 | model of | platelet-type bleeding disorder 3 | 1 |
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Relationships