Disease-gene associations mined from literature

Human genes for prothrombin deficiency

Prothrombin deficiency [DOID:2235]

An autosomal recessive disease that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11.

Synonyms:  prothrombin deficiency,  DOID:2235,  prothrombin deficiencies,  hypoprothrombinemia,  hypoprothrombinemias ...

Linkouts:  OMIM