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Disease Ontology Browser
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory