Hemophilia B

rare

Hemophilia B is a form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor IX deficiency.

Identifiers: MONDO:0010604 OMIM:306900 Orphanet:98879
Causal genes: F9
Part of: Hemophilia Hemorrhagic disease Inherited blood coagulation disorder
Also known as: Christmas disease · congenital factor IX deficiency · congenital factor IX disorder · factor IX deficiency · haemophilia B Leyden

Subtypes

Disease	ID	Subtypes
Mild hemophilia B	MONDO:0015717
Moderately severe hemophilia B	MONDO:0015716
Severe hemophilia B	MONDO:0015715
Symptomatic form of hemophilia B in female carriers	MONDO:0015788

Rare disease

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