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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.


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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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory