inherited bleeding disorder, platelet-type platelet-type bleeding disorder 11 https://github.com/monarch-initiative/mondo/issues/7693 https://github.com/monarch-initiative/mondo/issues/9994 https://www.malacards.org/card/bleeding_disorder_platelet_type_11 UMLS:C3280120 NANDO:2200670 platelet-type bleeding disorder-11 DOID:0111057 GP6-related platelet disorder inherited bleeding disorder, platelet-type caused by mutation in GP6 OMIM:614201 Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the GP6 gene, the gene encoding platelet glycoprotein VI (GPVI), a critical collagen receptor. Affected individuals typically have mild to moderate bleeding, including epistaxis, easy bruising, menorrhagia, or postsurgical bleeding, despite normal platelet morphology. Laboratory findings include absent or markedly reduced GPVI expression, defective platelet activation and aggregation in response to collagen, prolonged bleeding time, and impaired collagen binding. BDPLT11 MEDGEN:481750 Orphanet:98885 SCTID:765977002 MONDO:0013623 GARD:0013293 platelet-type bleeding disorder 11 GP6 inherited bleeding disorder, platelet-type Bleeding diathesis due to glycoprotein VI deficiency