Hereditary bleeding disorders

Hereditary defects in coagulation factors form up this group.

Systematic

Hereditary diseases of the hematopoetic system and coagulopathies
	Aplastic anemia
	Autoimmune lymphoproliferative syndrome 5
	Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
	Disorders of cobalamin metabolism
	Familial erythrocytosis 2
	Familial hemophagocytic lymphohistiocytosis
	H syndrome
	Hereditary bleeding disorders
		Afibrinogenemia
			FGA
			FGB
			FGG
		Disturbances of vitamin K metabolism
			Combined deficiency of vitamin K-dependent clotting factors type 1
				GGCX
			Combined deficiency of vitamin K-dependent clotting factors type 2
				VKORC1
			Coumarin resistance
				CYP2A6
				CYP2C9
				CYP4F2
				VKORC1
			Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency
				GGCX
		Dysfibrinogenemia
			FGA
			FGB
			FGG
		Factor XII deficiency
			F12
		Factor XIII A subunit deficiency
			F13A1
		Factor XIII B subunit deficiency
			F13B
		Plasminogen activator inhibitor deficiency
			SERPINE1
	Hereditary malign blood disorders
	Inheritable platelet disorders
	MIRAGE syndrome
	Ovalocytosis
	Paroxysmal nocturnal hemoglobinuria
	Retinitis pigmentosa and erythrocytic microcytosis
	Thromboembolic diseases
	Vasculitis due to ADA2 deficiency

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