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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: 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.


Contributing Projects:
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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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory