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DOID:2235 - prothrombin deficiency
Disease Ontology 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.
Synonyms: Congenital factor II deficiency, Factor II deficiency, Hereditary factor II deficiency disease, hypoprothrombinemia
Xenbase Genes
:
f2
| MONDO:0013361 - congenital prothrombin deficiency |
| MIM:613679 - PROTHROMBIN DEFICIENCY, CONGENITAL |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
blood coagulation disease (is_a),
thrombophilia (is_a)