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DO Term : platelet-type bleeding disorder 3 [DOID:0111056] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
PT-VWD,
platelet type-von Willebrand disease,
BDPLT3,
ORDO:52530,
pseudo-von Willebrand disease,
ICD10CM:D69.8,
OMIM:177820,
von Willebrand disease platelet-type,
177820

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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