Term Name: | prothrombin deficiency |
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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 ) |