Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0111045 - platelet-type bleeding disorder 9

Disease Ontology 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.

Synonyms: BDPLT9, collagen platelet receptor deficiency, glycoprotein Ia deficiency, GP Ia deficiency

Xenbase Genes : itga2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013622 - platelet-type bleeding disorder 9


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), blood platelet disease (is_a)