About   Help   FAQ
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.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory