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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, GP Ia deficiency, collagen platelet receptor deficiency, glycoprotein Ia deficiency,
Echinobase Genes :
MIM:614200 - bleeding disorder, platelet-type, 9; bdplt9 |
Other Model Organisms: AGR, 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),
inherited blood coagulation disease (is_a)