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Hemophilia A

rare

The most common form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency.

Identifiers: MONDO:0010602 OMIM:134500 OMIM:306700 Orphanet:98878
Causal genes: F8
Part of: X-linked disease Hemophilia Hemorrhagic disease Inherited blood coagulation disorder
Also known as: autosomal haemophilia a · classic haemophilia · classic hemophilia · classical haemophilia · classical hemophilia

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Hemophilia A with vascular abnormality	MONDO:0010603
Mild hemophilia A	MONDO:0015721
Moderately severe hemophilia A	MONDO:0015720
Severe hemophilia A	MONDO:0015719
Symptomatic form of hemophilia A in female carriers	MONDO:0015787

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