Thrombasthenia of Glanzmann and Naegeli

Glanzmann thrombasthenia is a rare autosomal recessive bleeding disorder as a result of platelet's inability to bind fibrinogen and form clots. This failure is caused by glycoprotein IIb-IIIa complex deficiency. Underlying mutations can be found in two distinct genes, ITGA2B and ITGB3.

Systematic

Inheritable platelet disorders
	Alloimmune thrombocytopenia
	Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia
	Bernard-Soulier syndrome
	Bleeding disorder platelet-type 9
	Glycoprotein 1a deficiency
	IVIC syndrome
	MYH9 related disorders
	Mediterranean macrothrombocytopenia
	Thrombasthenia of Glanzmann and Naegeli
		ITGA2B
		ITGB3
	Thrombocythemia 3
	Wiskott–Aldrich syndrome