platelet-type bleeding disorder 11 (DOID:0111057)
Alliance: disease page
Synonyms: BDPLT11; glycoprotein VI deficiency; GP VI deficiency
Alt IDs: OMIM:614201, ICD10CM:D69.8, ORDO:98885
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.