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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: An inherited blood coagulation 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory