Disease-gene associations mined from literature

Human genes for hemophilia B

Hemophilia B [DOID:12259]

An inherited blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.

Synonyms:  hemophilia B,  DOID:12259,  Congenital factor IX deficiency,  Congenital factor IX disorder,  deficiency, functional factor IX ...

Linkouts:  OMIM