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Disease Ontology Browser
prothrombin deficiency (DOID:2235)
Alliance: disease page
Synonyms: Congenital factor II deficiency; Factor II deficiency; Hereditary factor II deficiency disease; hypoprothrombinemia
Alt IDs: OMIM:613679, MESH:C562724, NCI:C26799, ORDO:325, UMLS_CUI:C0272317
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory