Human genes for prothrombin deficiency
Prothrombin deficiency [DOID:2235]
A thrombophilia 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