|  Help  |  About  |  Contact Us

DO Term : platelet-type bleeding disorder 9 [DOID:0111045] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • OMIM:614200,
  • GP Ia deficiency,
  • ICD10CM:D69.8,
  • glycoprotein Ia deficiency,
  • 614200,
  • ORDO:98886,
  • collagen platelet receptor deficiency,
  • BDPLT9
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents