About   Help   FAQ
Disease Ontology Browser
platelet-type bleeding disorder 9 (DOID:0111045)
Alliance: disease page
Synonyms: BDPLT9; collagen platelet receptor deficiency; glycoprotein Ia deficiency; GP Ia deficiency
Alt IDs: OMIM:614200, ICD10CM:D69.8, ORDO:98886
Definition: A blood platelet disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has_material_basis_in mutation in the ITGA2 gene on chromosome 5q11.2.

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
11/12/2024
MGI 6.24 		The Jackson Laboratory