Term Name:	prothrombin deficiency
Synonyms:	Congenital factor II deficiency, Factor II deficiency, Hereditary factor II deficiency disease, hypoprothrombinemia
Definition:	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.
Ontology:	Human Disease [DOID:2235]   ( DOID:2235 )