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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: An inherited blood coagulation 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)
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last database update
07/09/2019
MGI 6.14
The Jackson Laboratory