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DOID:2222 - factor X deficiency
Disease Ontology Definition:A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood.
Synonyms: Factor X deficiency, Factor X deficiency (disorder), disease, Stuart-Prower,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009212 - congenital factor X deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee