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Summary Literature (0)
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: disease, Stuart-Prower, Factor X deficiency, Factor X deficiency (disorder)

Xenbase Genes : f10

Mondo Disease Ontology (on Monarch Initiative):
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
Parent(s): autosomal recessive disease (is_a), blood coagulation disease (is_a)