Term Name:	platelet-type bleeding disorder 11
Synonyms:	BDPLT11, glycoprotein VI deficiency, GP VI deficiency
Definition:	A blood platelet disease characterized by autosomal recessive inheritance of mild to moderate bleeding and defective platelet activation and aggregation in response to collagen that has_material_basis_in compound heterozygous mutation in the GP6 gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0111057]   ( DOID:0111057 )