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Metadata
ID	DOID:0111057
Name	platelet-type bleeding disorder 11
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. https://www.ncbi.nlm.nih.gov/pubmed/19549989, https://www.ncbi.nlm.nih.gov/pubmed/19552682
Xrefs	ICD10CM:D69.8 OMIM:614201 ORDO:98885
Subsets	DO_rare_slim
Synonyms	BDPLT11 [EXACT] glycoprotein VI deficiency [EXACT] GP VI deficiency [EXACT]
Parent Relationships	is_a blood platelet disease is_a autosomal recessive disease